Canonical Allele Identifier: PA2827877777
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1792785
ClinVar RCV Id: RCV002455763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341508.1:p.Phe782Leu
CA354815872
NM_001354579.2:c.2346T>G
CA354815879
NM_001354579.2:c.2346T>A
CA354815894
NM_001354579.2:c.2344T>C