Canonical Allele Identifier: PA2828474665
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361173.1:p.Gly509Ser
CA16602534
NM_001374244.1:c.1525_1526delinsTC
CA168090454
NM_001374244.1:c.1525_1527delinsAGT
CA168090462
NM_001374244.1:c.1525_1527delinsAGC