Canonical Allele Identifier: PA2828778023
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Val563Gly
CA281998
NM_001378471.1:c.1688T>G