Canonical Allele Identifier: PA2828776980
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Thr207Lys
CA261663
NM_001378470.1:c.620C>A