Canonical Allele Identifier: PA2828776502
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gly442Ala
CA281965
NM_001378469.1:c.1325G>C