Allele Registry

Canonical Allele Identifier: PA343734

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032543

RCV003887877

ClinVar Variation:

39266

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Leu173Trp	CA343733 NM_207352.4:c.518T>G