Allele Registry

Canonical Allele Identifier: PA1139699048

Gene: CYP17A1 HGNC NCBI

ClinVar RCV:

RCV001106935

ClinVar Variation:

879432

HGVS (amino-acid)	Matching Registered Transcripts
NP_000093.1:p.Gly138Ser	CA377940301 NM_000102.4:c.412G>A