Canonical Allele Identifier: PA261665
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Thr241Lys
CA261663
NM_004333.6:c.722C>A