Canonical Allele Identifier: PA2828778052
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13981
ClinVar Variation Id: 162797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Asp601Glu
CA279981
NM_001378471.1:c.1803T>A
CA280051
NM_001378471.1:c.1803T>G