Allele Registry

Canonical Allele Identifier: PA119591

Gene: CYP2C9 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.781585976

Score 0.445326567

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000008916

RCV000008917

RCV000008918

RCV000008919

RCV000339502

RCV000787930

RCV000788094

RCV000788100

ClinVar Variation:

8408

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000762.2:p.Ile359Leu	CA119590 NM_000771.4:c.1075A>C