Canonical Allele Identifier: PA2827883304
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711755
ClinVar RCV Id: RCV002293300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Leu441Phe
CA369589052
NM_001354609.2:c.1321C>T