Allele Registry

Canonical Allele Identifier: PA658712984

Gene: SRD5A2 HGNC NCBI

ClinVar Allele:

485705

ClinVar RCV:

RCV000583779

ClinVar Variation:

492897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000339.2:p.Ala69Ser	CA346598903 NM_000348.4:c.205G>T