Canonical Allele Identifier: PA2828778005
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13969
ClinVar RCV Id: RCV000015003 RCV000030948 RCV000033333 RCV000208539 RCV000419516 RCV000426915 RCV000437189 RCV000505705 RCV001813207 RCV002271369 RCV002513056
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Leu560Val
CA123651
NM_001378471.1:c.1678C>G