Allele Registry

Canonical Allele Identifier: PA111217

Gene: CYP4V2 HGNC NCBI

ClinVar Allele:

17229

ClinVar RCV:

RCV000002274

ClinVar Variation:

2190

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Gly61Ser	CA339957 NM_207352.4:c.181G>A