Canonical Allele Identifier: PA2828776633
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711064
ClinVar RCV Id: RCV002292351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Lys569Glu
CA369543204
NM_001378469.1:c.1705A>G