Canonical Allele Identifier: PA645466290
Gene: FBXW7 HGNC NCBI

Linked Data

ClinVar Variation Id: 376421
ClinVar RCV Id: RCV000419083 RCV000418015 RCV000424541 RCV000425643 RCV000427761 RCV000429417 RCV000434540 RCV000435692 RCV000435934 RCV000440513 RCV000442879 RCV000443948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_361014.1:p.Arg479Leu
CA16602858
NM_033632.3:c.1436G>T