Canonical Allele Identifier: PA2828779812
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711778
ClinVar RCV Id: RCV002293323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.His477Pro
CA369588826
NM_001378474.1:c.1430A>C