Canonical Allele Identifier: PA2828775117
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711054
ClinVar RCV Id: RCV002292341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Pro456Leu
CA369588964
NM_001378467.1:c.1367C>T