Canonical Allele Identifier: PA2828779266
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13981
ClinVar Variation Id: 162797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Asp586Glu
CA279981
NM_001378473.1:c.1758T>A
CA280051
NM_001378473.1:c.1758T>G