Canonical Allele Identifier: PA2580536300
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1985912
ClinVar RCV Id: RCV002785792
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Arg257His
CA9269697
NM_173483.4:c.770G>A