Canonical Allele Identifier: PA340082
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.His231Arg
CA340081
NM_000348.4:c.692A>G