Canonical Allele Identifier: PA135081
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44801
ClinVar RCV Id: RCV000037915 RCV000428876
ClinVar Variation Id: 2501901
ClinVar RCV Id: RCV003228320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Gly466Arg
CA135079
NM_004333.6:c.1396G>A
CA168090546
NM_004333.6:c.1396G>C