Canonical Allele Identifier: PA356349
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 219484
ClinVar RCV Id: RCV000206668 RCV000566874 RCV001354647 RCV002288821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile1792Thr
CA350670
NM_000051.4:c.5375T>C