Canonical Allele Identifier: PA2828780399
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44802
ClinVar RCV Id: RCV000037918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Gly381del
CA135082
NM_001378475.1:c.1141_1143del
CA175340
NM_001378475.1:c.1141G>T