Canonical Allele Identifier: PA645374822
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372518
ClinVar Variation Id: 830332
ClinVar RCV Id: RCV001030762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Gly34Arg
CA45142058
NM_000348.4:c.100G>A
CA346599107
NM_000348.4:c.100G>C