Canonical Allele Identifier: PA2828776501
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 279992
ClinVar RCV Id: RCV000304268
ClinVar Variation Id: 372572
ClinVar RCV Id: RCV000413557 RCV000429423 RCV000824916 RCV000694211 RCV002291625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gly442Arg
CA10602955
NM_001378469.1:c.1324G>C
CA16042578
NM_001378469.1:c.1324G>A