Canonical Allele Identifier: PA2828778430
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711755
ClinVar RCV Id: RCV002293300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Leu389Phe
CA369589052
NM_001378472.1:c.1165C>T