Canonical Allele Identifier: PA1139730020
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 566595
ClinVar RCV Id: RCV000686444 RCV001027152 RCV003235347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2695del
CA645598125
NM_001351834.2:c.8082_8084del