Canonical Allele Identifier: PA093869
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40347
ClinVar Variation Id: 40348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Leu245Phe
CA280027
NM_004333.6:c.735A>C
CA280029
NM_004333.6:c.735A>T