Canonical Allele Identifier: PA2828780188
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40347
ClinVar Variation Id: 40348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Leu157Phe
CA280027
NM_001378475.1:c.471A>C
CA280029
NM_001378475.1:c.471A>T