Canonical Allele Identifier: PA2828775769
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 372627
ClinVar RCV Id: RCV000413389 RCV000764691 RCV001865287 RCV001813468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Arg389His
CA4516795
NM_001378468.1:c.1166G>A