Allele Registry

Canonical Allele Identifier: PA915965186

Gene: CYP2C9 HGNC NCBI

ClinVar RCV:

RCV000952677

ClinVar Variation:

773002

HGVS (amino-acid)	Matching Registered Transcripts
NP_000762.2:p.His251Arg	CA5617178 NM_000771.4:c.752A>G