Canonical Allele Identifier: PA658662708
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 459644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Tyr235Phe
CA1599849
NM_000348.4:c.704A>T