Allele Registry

Canonical Allele Identifier: PA105002

Gene: CYP4F22 HGNC NCBI

ClinVar RCV:

RCV000000957

RCV000412942

RCV001582456

ClinVar Variation:

909

HGVS (amino-acid)	Matching Registered Transcripts
NP_775754.2:p.His435Tyr	CA114616 NM_173483.4:c.1303C>T