Canonical Allele Identifier: PA2828778870
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40347
ClinVar RCV Id: RCV000033283 RCV000037956 RCV000171142 RCV000469440 RCV000515291 RCV000788013
ClinVar Variation Id: 40348
ClinVar RCV Id: RCV000033284 RCV000055897 RCV000037957 RCV000688777 RCV000788012 RCV002273939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Leu193Phe
CA280027
NM_001378473.1:c.579A>C
CA280029
NM_001378473.1:c.579A>T