Allele Registry

Canonical Allele Identifier: PA2573317547

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV002046572

ClinVar Variation:

1522486

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Glu437Lys	CA3162824 NM_207352.4:c.1309G>A