Canonical Allele Identifier: PA2741816205
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3045745
ClinVar RCV Id: RCV003951460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Phe223Leu
CA346597895
NM_000348.4:c.669C>G
CA346597896
NM_000348.4:c.669C>A
CA346597901
NM_000348.4:c.667T>C