Canonical Allele Identifier: PA2828779799
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44802
ClinVar RCV Id: RCV000037918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Gly469del
CA135082
NM_001378474.1:c.1405_1407del
CA175340
NM_001378474.1:c.1405G>T