Allele Registry

Canonical Allele Identifier: PA2828776628

Gene: BRAF HGNC NCBI

ClinVar RCV:

RCV000420521

RCV000431213

ClinVar Variation:

376292

376293

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365398.1:p.Asp565Glu	CA16602740 NM_001378469.1:c.1695C>G CA16602741 NM_001378469.1:c.1695C>A