Canonical Allele Identifier: PA658712984
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 492897
ClinVar RCV Id: RCV000583779
JSON-LD

Amino-acid Alleles

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