Canonical Allele Identifier: PA2828780396
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Gly381Ser
CA16602534
NM_001378475.1:c.1141_1142delinsTC
CA168090454
NM_001378475.1:c.1141_1143delinsAGT
CA168090462
NM_001378475.1:c.1141_1143delinsAGC