Canonical Allele Identifier: PA119591
Gene: CYP2C9 HGNC NCBI

Linked Data

ClinVar Variation Id: 8408
ClinVar RCV Id: RCV000008916 RCV000008917 RCV000008918 RCV000008919 RCV000339502 RCV000788094 RCV000787930 RCV000788100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000762.2:p.Ile359Leu
CA119590
NM_000771.4:c.1075A>C