Canonical Allele Identifier: PA658826366
Gene: CYP2C8 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000761.3:p.Arg139Lys
CA5617795
NM_000770.3:c.416G>A