Canonical Allele Identifier: PA261659
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44804
ClinVar RCV Id: RCV000037920 RCV000681421
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Thr470Arg
CA261657
NM_004333.6:c.1409C>G