Allele Registry

Canonical Allele Identifier: PA2580570948

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV002299070

ClinVar Variation:

1714695

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Ser257Arg	CA358948088 NM_207352.4:c.769A>C CA358948092 NM_207352.4:c.771C>A CA358948093 NM_207352.4:c.771C>G