Canonical Allele Identifier: PA224885
Gene: SRD5A2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Ala51Thr
CA224884
NM_000348.4:c.151G>A