Canonical Allele Identifier: PA2828474668
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44802
ClinVar RCV Id: RCV000037918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361173.1:p.Gly509del
CA135082
NM_001374244.1:c.1525_1527del
CA175340
NM_001374244.1:c.1525G>T