Canonical Allele Identifier: PA2828778914
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1709831
ClinVar RCV Id: RCV002290173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Ser262Thr
CA369590384
NM_001378473.1:c.784T>A