Canonical Allele Identifier: PA2828779076
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1163474
ClinVar RCV Id: RCV001508597
ClinVar Variation Id: 1711081
ClinVar RCV Id: RCV002292368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Phe416Leu
CA369588879
NM_001378473.1:c.1248T>G
CA369588880
NM_001378473.1:c.1248T>A
CA369588884
NM_001378473.1:c.1246T>C