Canonical Allele Identifier: PA2828780466
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 29808
ClinVar Variation Id: 265358
ClinVar RCV Id: RCV000255590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Trp443Cys
CA250333
NM_001378475.1:c.1329G>C
CA10588419
NM_001378475.1:c.1329G>T