Canonical Allele Identifier: PA2828776660
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13969
ClinVar RCV Id: RCV000015003 RCV000030948 RCV000033333 RCV000208539 RCV000419516 RCV000426915 RCV000437189 RCV000505705 RCV001813207 RCV002271369 RCV002513056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Leu575Val
CA123651
NM_001378469.1:c.1723C>G