Canonical Allele Identifier: PA2828775138
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Gly467Val
CA135076
NM_001378467.1:c.1400G>T