Canonical Allele Identifier: PA2499300785
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1146419
ClinVar RCV Id: RCV001485641
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Ala23Val
CA9269452
NM_173483.4:c.68C>T