Allele Registry

Canonical Allele Identifier: PA2573317560

Gene: CYP4V2 HGNC NCBI

ClinVar Variation Id: 1493877

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Phe460Leu	CA358950663 NM_207352.4:c.1378T>C CA358950668 NM_207352.4:c.1380C>A CA358950669 NM_207352.4:c.1380C>G