Canonical Allele Identifier: PA2741866770
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2804810
ClinVar RCV Id: RCV003606095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1256Ser
CA6265350
NM_001351834.2:c.3767T>G