Allele Registry

Canonical Allele Identifier: PA111237

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000002272

RCV001047112

ClinVar Variation:

2188

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Ile111Thr	CA339955 NM_207352.4:c.332T>C