Canonical Allele Identifier: PA2828779798
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13974
ClinVar RCV Id: RCV000015008 RCV000033307 RCV000212152 RCV000211748 RCV000419555 RCV000427006 RCV000427215 RCV000419576 RCV000437869 RCV000434590 RCV000443381 RCV000506575 RCV000424773 RCV000436804 RCV001813209 RCV002287336 RCV003450641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Gly469Glu
CA279970
NM_001378474.1:c.1406G>A