NM_001382273.1(TNK2):c.2651T>G (p.Leu884Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004473322.1
Allele description [Variation Report for NM_001382273.1(TNK2):c.2651T>G (p.Leu884Arg)]
NM_001382273.1(TNK2):c.2651T>G (p.Leu884Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
magnesium transporter NIPA2 isoform X1 [Rattus norvegicus]
magnesium transporter NIPA2 isoform X1 [Rattus norvegicus]gi|2678866481|ref|XP_063118441.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024