Canonical Allele Identifier: PA2828775877
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711045
ClinVar RCV Id: RCV002292332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Trp476Gly
CA369588836
NM_001378468.1:c.1426T>G