Canonical Allele Identifier: PA916033487
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 569948
ClinVar RCV Id: RCV000690712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr1810Ile
CA382544004
NM_001351834.2:c.5429C>T