Allele Registry

Canonical Allele Identifier: PA2742038059

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV003890944

ClinVar Variation:

3027690

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Phe433Leu	CA358950490 NM_207352.4:c.1297T>C CA358950494 NM_207352.4:c.1299C>A CA358950495 NM_207352.4:c.1299C>G