Allele Registry

Canonical Allele Identifier: PA645470724

Gene: CYP2C9 HGNC NCBI

ClinVar Allele:

227774

ClinVar RCV:

RCV000308849

RCV000787931

RCV000788095

RCV000788101

ClinVar Variation:

225984

HGVS (amino-acid)	Matching Registered Transcripts
NP_000762.2:p.Asp360Glu	CA5617301 NM_000771.4:c.1080C>G CA5617302 NM_000771.4:c.1080C>A