Canonical Allele Identifier: PA281997
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40388
ClinVar RCV Id: RCV000033334 RCV000433036 RCV000440873 RCV000824927 RCV001172273 RCV001705626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Thr599Ile
CA281995
NM_004333.6:c.1796C>T