Allele Registry

Canonical Allele Identifier: PA658828334

Gene: CYP4F22 HGNC NCBI

ClinVar RCV:

RCV000678419

ClinVar Variation:

560325

HGVS (amino-acid)	Matching Registered Transcripts
NP_775754.2:p.Arg362Gly	CA404539376 NM_173483.4:c.1084C>G