Canonical Allele Identifier: PA1139743302
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13966
ClinVar RCV Id: RCV000015000 RCV000014999 RCV000037938 RCV000423181 RCV000440232 RCV000433498 RCV000443528 RCV000422559 RCV000425399 RCV000432202 RCV000440872 RCV000432849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Lys641Glu
CA123645
NM_001374258.1:c.1921A>G