Allele Registry

Canonical Allele Identifier: PA273327

Gene: CYP4V2 HGNC NCBI

ClinVar Allele:

177092

ClinVar RCV:

RCV000153133

ClinVar Variation:

166978

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Arg465Gly	CA273326 NM_207352.4:c.1393A>G