Allele Registry

Canonical Allele Identifier: PA2828776632

Gene: BRAF HGNC NCBI

ClinVar RCV:

RCV000413430

ClinVar Variation:

372757

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365398.1:p.Thr567Pro	CA16042558 NM_001378469.1:c.1699A>C