Canonical Allele Identifier: PA2828776469
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711755
ClinVar RCV Id: RCV002293300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Leu419Phe
CA369589052
NM_001378469.1:c.1255C>T