Canonical Allele Identifier: PA2828776637
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40386
ClinVar RCV Id: RCV000033331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Ile570Thr
CA281992
NM_001378469.1:c.1709T>C