Canonical Allele Identifier: PA2741828408
Gene: CYP4F2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2606567
ClinVar RCV Id: RCV004348872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073.3:p.Arg57Gln
CA305909544
NM_001082.5:c.170G>A