Canonical Allele Identifier: PA2827883346
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1905687
ClinVar RCV Id: RCV002583696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Ser467Leu
CA168090516
NM_001354609.2:c.1400C>T