Allele Registry

Canonical Allele Identifier: PA343709

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032528

RCV001358595

ClinVar Variation:

39251

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg390His	CA343708 NM_207352.4:c.1169G>A