Canonical Allele Identifier: PA2828778913
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 2066349
ClinVar RCV Id: RCV002949048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Leu260Val
CA369590395
NM_001378473.1:c.778C>G