Allele Registry

Canonical Allele Identifier: PA343715

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032531

RCV000659009

ClinVar Variation:

39254

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg400His	CA343714 NM_207352.4:c.1199G>A