Canonical Allele Identifier: PA2580204739
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1747998
ClinVar RCV Id: RCV002351688 RCV003605806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr1835Ile
CA382545684
NM_001351834.2:c.5504C>T