Allele Registry

Canonical Allele Identifier: PA284659

Gene: BRAF HGNC NCBI

ClinVar RCV:

RCV000422257

RCV000425037

RCV000431645

RCV000433029

RCV000439352

RCV000441971

RCV001363294

RCV003390750

ClinVar Variation:

55794

HGVS (amino-acid)	Matching Registered Transcripts
NP_004324.2:p.Asn581His	CA284657 NM_004333.6:c.1741A>C