Canonical Allele Identifier: PA1139744758
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13973
ClinVar RCV Id: RCV000015007 RCV000033289 RCV000080904 RCV000208766 RCV001027771 RCV001261967 RCV001329219 RCV001813208 RCV001813744 RCV004018628 RCV003224098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Gln260Arg
CA222583
NM_001378467.1:c.779A>G