Canonical Allele Identifier: PA2741867511
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2859094
ClinVar RCV Id: RCV003605391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser2310Cys
CA228412694
NM_001351834.2:c.6928A>T