Canonical Allele Identifier: PA2828778619
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 76687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Leu545Gln
CA16602257
NM_001378472.1:c.1634T>A