NM_018194.6(HHAT):c.997G>A (p.Gly333Arg) AND Chondrodysplasia-pseudohermaphroditism syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002505480.1
Allele description [Variation Report for NM_018194.6(HHAT):c.997G>A (p.Gly333Arg)]
NM_018194.6(HHAT):c.997G>A (p.Gly333Arg)
Condition(s)
Assertion and evidence details
Last Updated: May 12, 2024