Allele Registry

Canonical Allele Identifier: PA645376472

Gene: CYP4V2 HGNC NCBI

ClinVar Variation Id: 348299

HGVS (amino-acid)	Matching Registered Transcripts
NP_997235.3:p.Ala101Val	CA3162494 NM_207352.4:c.302C>T