Canonical Allele Identifier: PA658713009
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 492899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Tyr91His
CA1599996
NM_000348.4:c.271T>C