Canonical Allele Identifier: PA2828778719
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 162795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Ala660Asp
CA273127
NM_001378472.1:c.1979C>A