Canonical Allele Identifier: PA135078
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Gly464Val
CA135076
NM_004333.6:c.1391G>T