Canonical Allele Identifier: PA2741878256
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 2633111
ClinVar RCV Id: RCV003408428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Phe293Leu
CA369590537
NM_001378467.1:c.879T>G
CA369590538
NM_001378467.1:c.879T>A
CA369590543
NM_001378467.1:c.877T>C