Canonical Allele Identifier: PA2826224972
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_001185783.1:p.Ile39Thr
CA377682933
NM_001198854.1:c.116T>C