Canonical Allele Identifier: PA2580102976
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2390634
ClinVar RCV Id: RCV002714702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Glu248Lys
CA5669486
NM_000102.4:c.742G>A