Canonical Allele Identifier: PA2580102973
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2439628
ClinVar RCV Id: RCV003143879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Arg239Gln
CA5669490
NM_000102.4:c.716G>A