Canonical Allele Identifier: PA916034136
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481318
ClinVar RCV Id: RCV000573776 RCV000705568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met2315Thr
CA382557267
NM_001351834.2:c.6944T>C