Canonical Allele Identifier: PA658662700
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 459642
ClinVar RCV Id: RCV000540681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Ala228Val
CA346597874
NM_000348.4:c.683C>T