Canonical Allele Identifier: PA658712956
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 492895
ClinVar RCV Id: RCV000583658 RCV001591351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Leu20Pro
CA1600035
NM_000348.4:c.59T>C