Canonical Allele Identifier: PA2825034995
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1707973
ClinVar RCV Id: RCV002287134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2252Ile
CA382555300
NM_000051.4:c.6755C>T