Canonical Allele Identifier: PA1139729663
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 939539
ClinVar RCV Id: RCV001208957 RCV004033751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2608Ala
CA382561309
NM_001351834.2:c.7822A>G