Allele Registry

Canonical Allele Identifier: PA2573317542

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV001905158

ClinVar Variation:

1363936

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Val420Ile	CA112135002 NM_207352.4:c.1258G>A