Canonical Allele Identifier: PA2828777194
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376072
ClinVar RCV Id: RCV000421677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Gly435Ser
CA16602534
NM_001378470.1:c.1303_1304delinsTC
CA168090454
NM_001378470.1:c.1303_1305delinsAGT
CA168090462
NM_001378470.1:c.1303_1305delinsAGC