Canonical Allele Identifier: PA2827883389
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13975
ClinVar Variation Id: 177844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Leu485Phe
CA273414
NM_001354609.2:c.1455G>C
CA280060
NM_001354609.2:c.1455G>T