Canonical Allele Identifier: PA916033332
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453557
ClinVar RCV Id: RCV000525974 RCV000572412 RCV001584234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1681Thr
CA382540369
NM_001351834.2:c.5042T>C