Canonical Allele Identifier: PA1139743291
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13972
ClinVar RCV Id: RCV000015006 RCV000037932 RCV000418680 RCV000423919 RCV000426107 RCV000433779 RCV000437006 RCV000426339 RCV000435875 RCV000443065 RCV000443882 RCV001238853 RCV000442759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Asp634Gly
CA123657
NM_001374258.1:c.1901A>G