Canonical Allele Identifier: PA2828775660
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 2120966
ClinVar RCV Id: RCV003048923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Arg252Gly
CA369590814
NM_001378468.1:c.754C>G