Canonical Allele Identifier: PA2828777997
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 177672
ClinVar RCV Id: RCV000154266 RCV000157825 RCV000445270 RCV000426478 RCV000522002
ClinVar Variation Id: 180789
ClinVar RCV Id: RCV000157824 RCV000437147 RCV001212304
ClinVar Variation Id: 202193
ClinVar RCV Id: RCV000184039 RCV000414439 RCV000427091 RCV002222430 RCV002291588 RCV002516942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Phe558Leu
CA280058
NM_001378471.1:c.1674T>G
CA280071
NM_001378471.1:c.1672T>C
CA295915
NM_001378471.1:c.1674T>A