Allele Registry

Canonical Allele Identifier: PA2828776648

Gene: BRAF HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000154266

RCV000157824

RCV000157825

RCV000184039

RCV000414439

RCV000426478

RCV000427091

RCV000437147

RCV000445270

RCV000522002

RCV001212304

RCV002222430

RCV002291588

RCV002516942

ClinVar Variation:

177672

180789

202193

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365398.1:p.Phe573Leu	CA280058 NM_001378469.1:c.1719T>G CA280071 NM_001378469.1:c.1717T>C CA295915 NM_001378469.1:c.1719T>A