Canonical Allele Identifier: PA2828779796
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Gly469Ser
CA16602534
NM_001378474.1:c.1405_1406delinsTC
CA168090454
NM_001378474.1:c.1405_1407delinsAGT
CA168090462
NM_001378474.1:c.1405_1407delinsAGC