Canonical Allele Identifier: PA645374841
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 335817
ClinVar RCV Id: RCV000280741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Cys88Trp
CA10615096
NM_000348.4:c.264C>G