Canonical Allele Identifier: PA2825252877
Gene: CYP2C8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2559398
ClinVar RCV Id: RCV004329684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000761.3:p.Ile141Thr
CA377682933
NM_000770.3:c.422T>C