Canonical Allele Identifier: PA2580203340
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2104460
ClinVar RCV Id: RCV003031387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val723Met
CA382538783
NM_001351834.2:c.2167G>A