Canonical Allele Identifier: PA094029
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13961
ClinVar Variation Id: 376069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Val600Glu
CA123643
NM_004333.6:c.1799T>A
CA16602531
NM_004333.6:c.1799_1800delinsAA