Canonical Allele Identifier: PA2828776362
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 2833434
ClinVar RCV Id: RCV003655853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Ile300Leu
CA369590469
NM_001378469.1:c.898A>T
CA369590470
NM_001378469.1:c.898A>C