Canonical Allele Identifier: PA2827877816
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 3221092
ClinVar RCV Id: RCV004507948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341508.1:p.Asp819Val
CA2650299
NM_001354579.2:c.2456A>T