Canonical Allele Identifier: PA2828474978
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44813
ClinVar Variation Id: 375948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361173.1:p.Asp634Asn
CA135095
NM_001374244.1:c.1900G>A
CA16602427
NM_001374244.1:c.1899_1900delinsGA