Canonical Allele Identifier: PA2828775131
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13963
ClinVar RCV Id: RCV000014996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Ile466Ser
CA250634
NM_001378467.1:c.1397T>G