Canonical Allele Identifier: PA2828775421
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 422080
ClinVar RCV Id: RCV000486116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Ile758Ser
CA16618359
NM_001378467.1:c.2273_2274delinsGT
CA369537050
NM_001378467.1:c.2273T>G