Canonical Allele Identifier: PA2828779960
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Lys601Ile
CA282001
NM_001378474.1:c.1802A>T