Canonical Allele Identifier: PA2828474960
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376071
ClinVar RCV Id: RCV000427646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361173.1:p.Ile632Val
CA16602533
NM_001374244.1:c.1894A>G