Allele Registry

Canonical Allele Identifier: PA645376575

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000351328

RCV000392054

RCV002523469

ClinVar Variation:

348305

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg221Cys	CA3162617 NM_207352.4:c.661C>T