Canonical Allele Identifier: PA2580202549
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1768709
ClinVar RCV Id: RCV002382926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr332Asp
CA382531302
NM_001351834.2:c.994T>G