Allele Registry

Canonical Allele Identifier: PA645376608

Gene: CYP4V2 HGNC NCBI

ClinVar Allele:

251428

ClinVar RCV:

RCV000245860

RCV000333143

RCV000387735

RCV001523281

ClinVar Variation:

263298

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Glu275Lys	CA3162674 NM_207352.4:c.823G>A