Canonical Allele Identifier: PA645380890
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 328438
ClinVar RCV Id: RCV000382663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Gln288Lys
CA9269721
NM_173483.4:c.862C>A