Allele Registry

Canonical Allele Identifier: PA2828776534

Gene: BRAF HGNC NCBI

ClinVar RCV:

RCV002293323

ClinVar Variation:

1711778

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365398.1:p.His455Pro	CA369588826 NM_001378469.1:c.1364A>C