Allele Registry

Canonical Allele Identifier: PA343727

Gene: CYP4V2 HGNC NCBI

ClinVar Allele:

47867

3398423

ClinVar RCV:

RCV000032538

RCV001221420

RCV003887876

RCV004575919

ClinVar Variation:

39261

3239433

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Gly95Arg	CA343726 NM_207352.4:c.283G>A CA358946944 NM_207352.4:c.283G>C