Canonical Allele Identifier: PA2741809158
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2972671
ClinVar RCV Id: RCV003837781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Phe435Ser
CA377938260
NM_000102.4:c.1304T>C