Canonical Allele Identifier: PA2828777862
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Phe431Ser
CA280002
NM_001378471.1:c.1292T>C