Canonical Allele Identifier: PA2828777865
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44802
ClinVar RCV Id: RCV000037918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Gly432del
CA135082
NM_001378471.1:c.1294_1296del
CA175340
NM_001378471.1:c.1294G>T