Canonical Allele Identifier: PA2828776785
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 422080
ClinVar RCV Id: RCV000486116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Ile733Ser
CA16618359
NM_001378469.1:c.2198_2199delinsGT
CA369537050
NM_001378469.1:c.2198T>G