Canonical Allele Identifier: PA1139743296
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Leu637Val
CA123651
NM_001374258.1:c.1909C>G