Canonical Allele Identifier: PA658828324
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 560311
ClinVar RCV Id: RCV000678402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Arg283Trp
CA9269714
NM_173483.4:c.847C>T