Allele Registry

Canonical Allele Identifier: PA2580570919

Gene: CYP4V2 HGNC NCBI

ClinVar RCV:

RCV002691107

ClinVar Variation:

1958068

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Pro98Ser	CA358946961 NM_207352.4:c.292C>T