Canonical Allele Identifier: PA1139744746
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 178963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Ile211Val
CA183392
NM_001378467.1:c.631A>G