Canonical Allele Identifier: PA2741867382
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2585047
ClinVar RCV Id: RCV003340947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2131Pro
CA382553337
NM_001351834.2:c.6391G>C