Canonical Allele Identifier: PA891866347
Gene: FBXW7 HGNC NCBI

Linked Data

ClinVar Variation Id: 376424
ClinVar RCV Id: RCV000418253 RCV000420626 RCV000421948 RCV000423047 RCV000428507 RCV000429608 RCV000428228 RCV000433338 RCV000434990 RCV000438226 RCV000439833 RCV000439579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336727.1:p.Arg505Leu
CA16602860
NM_001349798.2:c.1514G>T