Canonical Allele Identifier: PA2573162624
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1404776
ClinVar RCV Id: RCV001901815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000093.1:p.Ser210Thr
CA377939804
NM_000102.4:c.629G>C