Allele Registry

Canonical Allele Identifier: PA119595

Gene: CYP2C9 HGNC NCBI

ClinVar RCV:

RCV000008921

ClinVar Variation:

8410

HGVS (amino-acid)	Matching Registered Transcripts
NP_000762.2:p.Leu208Val	CA119594 NM_000771.4:c.622T>G