Canonical Allele Identifier: PA645374866
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Gln126Arg
CA1599952
NM_000348.4:c.377A>G