Allele Registry

Canonical Allele Identifier: PA2573317462

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV001929494

ClinVar Variation:

1426581

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Ile78Met	CA358946838 NM_207352.4:c.234T>G