Canonical Allele Identifier: PA645466294
Gene: FBXW7 HGNC NCBI

Linked Data

ClinVar Variation Id: 69961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_361014.1:p.Arg505Cys
CA16602253
NM_033632.3:c.1513C>T