Canonical Allele Identifier: PA2828776517
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gly447Ser
CA16602534
NM_001378469.1:c.1339_1340delinsTC
CA168090454
NM_001378469.1:c.1339_1341delinsAGT
CA168090462
NM_001378469.1:c.1339_1341delinsAGC