Canonical Allele Identifier: PA2828780398
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13970
ClinVar Variation Id: 177775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Gly381Arg
CA123653
NM_001378475.1:c.1141G>C
CA180746
NM_001378475.1:c.1141G>A