Canonical Allele Identifier: PA2827877781
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1793013
ClinVar RCV Id: RCV002433339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341508.1:p.Glu788Asp
CA354815742
NM_001354579.2:c.2364A>T
CA354815746
NM_001354579.2:c.2364A>C