Canonical Allele Identifier: PA1139733250
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 921875
ClinVar RCV Id: RCV001181583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys430Arg
CA382533532
NM_001351834.2:c.1288T>C