Allele Registry

Canonical Allele Identifier: PA2580570916

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV003051230

ClinVar Variation:

2142902

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Ile78del	CA112120918 NM_207352.4:c.232_234del