Canonical Allele Identifier: PA1139743260
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Phe508Ser
CA280002
NM_001374258.1:c.1523T>C