Canonical Allele Identifier: PA2827883526
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376284
ClinVar RCV Id: RCV000419349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Ser605Phe
CA16602732
NM_001354609.2:c.1813_1814delinsTT