Canonical Allele Identifier: PA2828778569
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40383
ClinVar Variation Id: 2769805
ClinVar RCV Id: RCV003540440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Asp513Glu
CA280016
NM_001378472.1:c.1539T>G
CA369544012
NM_001378472.1:c.1539T>A