Canonical Allele Identifier: PA2828777191
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Phe434Ser
CA280002
NM_001378470.1:c.1301T>C