Canonical Allele Identifier: PA658662678
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 459636
ClinVar RCV Id: RCV000537388 RCV001519907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Leu113Val
CA1599959
NM_000348.4:c.337C>G