Allele Registry

Canonical Allele Identifier: PA276933

Gene: CYP4V2 HGNC NCBI

ClinVar Allele:

206572

ClinVar RCV:

RCV000191926

ClinVar Variation:

209986

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Asn466Asp	CA276932 NM_207352.4:c.1396A>G