Canonical Allele Identifier: PA1139729637
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 921116
ClinVar RCV Id: RCV001180266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2605Val
CA382561288
NM_001351834.2:c.7813A>G