Canonical Allele Identifier: PA2580203338
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2118076
ClinVar RCV Id: RCV003030296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr714Asn
CA382538694
NM_001351834.2:c.2141C>A