Canonical Allele Identifier: PA2828775154
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Gly472Ser
CA16602534
NM_001378467.1:c.1414_1415delinsTC
CA168090454
NM_001378467.1:c.1414_1416delinsAGT
CA168090462
NM_001378467.1:c.1414_1416delinsAGC