Canonical Allele Identifier: PA2828779085
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711080
ClinVar RCV Id: RCV002292367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Thr418Ala
CA369588878
NM_001378473.1:c.1252A>G