Canonical Allele Identifier: PA2580205302
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1999645
ClinVar RCV Id: RCV002819752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2082Ile
CA382551800
NM_001351834.2:c.6245A>T