Canonical Allele Identifier: PA2573162640
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1457632
ClinVar RCV Id: RCV001953856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Gly436Arg
CA5669342
NM_000102.4:c.1306G>A
CA377938255
NM_000102.4:c.1306G>C