Canonical Allele Identifier: PA2828775857
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Phe468Ser
CA280002
NM_001378468.1:c.1403T>C