Canonical Allele Identifier: PA2580204033
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1718058
ClinVar RCV Id: RCV002296521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1432Ile
CA382531496
NM_001351834.2:c.4294G>A