Canonical Allele Identifier: PA2828778435
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711780
ClinVar RCV Id: RCV002293325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Asp393Tyr
CA369589028
NM_001378472.1:c.1177G>T