Canonical Allele Identifier: PA101288
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1456799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Ala174Glu
CA377940043
NM_000102.4:c.521C>A