Canonical Allele Identifier: PA2828777870
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Gly432Ser
CA16602534
NM_001378471.1:c.1294_1295delinsTC
CA168090454
NM_001378471.1:c.1294_1296delinsAGT
CA168090462
NM_001378471.1:c.1294_1296delinsAGC