Canonical Allele Identifier: PA916034531
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 577209
ClinVar RCV Id: RCV000699898 RCV002406616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2628Leu
CA382561435
NM_001351834.2:c.7882A>C