Canonical Allele Identifier: PA1139726695
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 935475
ClinVar RCV Id: RCV001204073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2142Ile
CA382553517
NM_001351834.2:c.6425C>T