Canonical Allele Identifier: PA2828776002
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13968
ClinVar RCV Id: RCV000015002 RCV000421775 RCV000421201 RCV000432024 RCV000439504 RCV000444137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Leu597Arg
CA123649
NM_001378468.1:c.1790T>G