Canonical Allele Identifier: PA340073
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3341
ClinVar RCV Id: RCV000003505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Gly183Ser
CA340072
NM_000348.4:c.547G>A