Canonical Allele Identifier: PA2580202529
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1768453
ClinVar RCV Id: RCV002387361 RCV003500761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg329Ile
CA382531220
NM_001351834.2:c.986G>T