Canonical Allele Identifier: PA2741937357
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2887235
ClinVar RCV Id: RCV003611390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036311.3:p.Met1Leu