Canonical Allele Identifier: PA2827883311
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711780
ClinVar RCV Id: RCV002293325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Asp445Tyr
CA369589028
NM_001354609.2:c.1333G>T