Canonical Allele Identifier: PA2580102958
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2238030
ClinVar RCV Id: RCV002729024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Val171Ile
CA377940064
NM_000102.4:c.511G>A