Canonical Allele Identifier: PA2829517519
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1163474
ClinVar RCV Id: RCV001508597
ClinVar Variation Id: 1711081
ClinVar RCV Id: RCV002292368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Phe468Leu
CA369588879
NM_004333.6:c.1404T>G
CA369588880
NM_004333.6:c.1404T>A
CA369588884
NM_004333.6:c.1402T>C