Canonical Allele Identifier: PA2828779827
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Leu485Ser
CA280052
NM_001378474.1:c.1454T>C