Canonical Allele Identifier: PA2828779080
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Gly417Ser
CA16602534
NM_001378473.1:c.1249_1250delinsTC
CA168090454
NM_001378473.1:c.1249_1251delinsAGT
CA168090462
NM_001378473.1:c.1249_1251delinsAGC