Allele Registry

Canonical Allele Identifier: PA119593

Gene: CYP2C9 HGNC NCBI

ClinVar RCV:

RCV000008920

RCV000309101

RCV000723560

RCV000787929

RCV000788093

RCV000788099

RCV001263463

ClinVar Variation:

8409

HGVS (amino-acid)	Matching Registered Transcripts
NP_000762.2:p.Arg144Cys	CA119592 NM_000771.4:c.430C>T CA356589 NM_000771.4:c.[430C>T;1075A=]