Canonical Allele Identifier: PA2580206626
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1761376
ClinVar RCV Id: RCV002416880 RCV003099800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2653Thr
CA382561709
NM_001351834.2:c.7958T>C