Canonical Allele Identifier: PA2580203314
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1784961
ClinVar RCV Id: RCV002419990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val682Ala
CA382537430
NM_001351834.2:c.2045T>C