Canonical Allele Identifier: PA2828776489
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gly438Glu
CA369588919
NM_001378469.1:c.1313G>A