Allele Registry

Canonical Allele Identifier: PA343704

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV000032525

RCV001852653

RCV003887875

ClinVar Variation:

39248

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Trp340Ter