Canonical Allele Identifier: PA2828776512
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Phe446Ser
CA280002
NM_001378469.1:c.1337T>C