Canonical Allele Identifier: PA340086
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3349
ClinVar RCV Id: RCV000003513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Glu197Asp
CA340085
NM_000348.4:c.591G>T
CA346598058
NM_000348.4:c.591G>C