Canonical Allele Identifier: PA2827883137
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40347
ClinVar Variation Id: 40348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Leu245Phe
CA280027
NM_001354609.2:c.735A>C
CA280029
NM_001354609.2:c.735A>T