Canonical Allele Identifier: PA645428947
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376071
ClinVar RCV Id: RCV000427646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Ile592Val
CA16602533
NM_004333.6:c.1774A>G