NM_001136193.2(FASTKD2):c.63G>A (p.Ala21=) AND FASTKD2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 15, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003950903.1
Allele description [Variation Report for NM_001136193.2(FASTKD2):c.63G>A (p.Ala21=)]
NM_001136193.2(FASTKD2):c.63G>A (p.Ala21=)
Condition(s)
- Name:
- FASTKD2-related disorder
- Synonyms:
- FASTKD2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 29, 2024