Canonical Allele Identifier: PA1139743256
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Gly504Val
CA135076
NM_001374258.1:c.1511G>T