Canonical Allele Identifier: PA2825317271
Gene: FBXW7 HGNC NCBI

Linked Data

ClinVar Variation Id: 376426
ClinVar RCV Id: RCV000419073 RCV000419711 RCV000420985 RCV000423791 RCV000429788 RCV000430339 RCV000431685 RCV000434480 RCV000440442 RCV000441048 RCV000441739 RCV000444420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001013433.1:p.Arg387Ser
CA16602862
NM_001013415.2:c.1159C>A