Allele Registry

Canonical Allele Identifier: PA2580570970

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV002890853

ClinVar Variation:

2040921

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Pro436Arg	CA358950513 NM_207352.4:c.1307C>G