Allele Registry

Canonical Allele Identifier: PA915965187

Gene: CYP2C9 HGNC NCBI

ClinVar RCV:

RCV000787934

RCV000788098

RCV000788104

RCV000835752

ClinVar Variation:

370010

HGVS (amino-acid)	Matching Registered Transcripts
NP_000762.2:p.Arg335Trp	CA5617278 NM_000771.4:c.1003C>T