Canonical Allele Identifier: PA2828778478
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375950
ClinVar RCV Id: RCV000429405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Gly417Leu
CA16602429
NM_001378472.1:c.1249_1250delinsTT
CA645556780
NM_001378472.1:c.1249_1250delinsCT