Canonical Allele Identifier: PA2742022412
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2985877
ClinVar RCV Id: RCV003841484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Gly290Trp
CA404536128
NM_173483.4:c.868G>T