Canonical Allele Identifier: PA2828779783
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376073
ClinVar RCV Id: RCV000424079 RCV000427285 RCV000434755 RCV000431475 RCV000437081 RCV000443232 RCV000442274 RCV001861476 RCV003128083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Gly466Glu
CA16602535
NM_001378474.1:c.1397G>A