Canonical Allele Identifier: PA115202
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1803
ClinVar RCV Id: RCV000001876 RCV001826403 RCV001376810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Arg125Gln
CA115201
NM_000102.4:c.374G>A