Canonical Allele Identifier: PA2828775274
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376071
ClinVar RCV Id: RCV000427646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Ile595Val
CA16602533
NM_001378467.1:c.1783A>G