Allele Registry

Canonical Allele Identifier: PA1139766100

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV001058545

ClinVar Variation:

853684

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Glu438Lys	CA3162825 NM_207352.4:c.1312G>A