Canonical Allele Identifier: PA2827883477
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376071
ClinVar RCV Id: RCV000427646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Ile592Val
CA16602533
NM_001354609.2:c.1774A>G