Canonical Allele Identifier: PA2499228507
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1066592
ClinVar RCV Id: RCV001377631 RCV003469628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Pro409Leu
CA5669370
NM_000102.4:c.1226C>T