Canonical Allele Identifier: PA261662
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44818
ClinVar RCV Id: RCV000037939 RCV000417689 RCV000434946 RCV000420107 RCV000431024 RCV000444564 RCV000425098 RCV000438200 RCV000999627 RCV003539772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Lys601Thr
CA261660
NM_004333.6:c.1802A>C