Allele Registry

Canonical Allele Identifier: PA1139766099

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV001206101

ClinVar Variation:

937144

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Pro436Leu	CA358950514 NM_207352.4:c.1307C>T