Canonical Allele Identifier: PA2741809160
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2681119
ClinVar RCV Id: RCV003468654 RCV003575109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Arg440Cys
CA377938232
NM_000102.4:c.1318C>T