Canonical Allele Identifier: PA101396
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1793
ClinVar RCV Id: RCV000001866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Asp116Val
CA115190
NM_000102.4:c.347A>T