Canonical Allele Identifier: PA658828325
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 560323
ClinVar RCV Id: RCV000678416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.Asp304Glu
CA404536324
NM_173483.4:c.912C>A
CA404536325
NM_173483.4:c.912C>G