Canonical Allele Identifier: PA645510534
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 440485
ClinVar RCV Id: RCV000508957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Tyr242Cys
CA346597764
NM_000348.4:c.725A>G