Canonical Allele Identifier: PA340080
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Gly196Ser
CA340079
NM_000348.4:c.586G>A