Canonical Allele Identifier: PA1139744761
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 840703
ClinVar RCV Id: RCV001042765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Glu278Asp
CA369590651
NM_001378467.1:c.834A>C
CA369590652
NM_001378467.1:c.834A>T