Canonical Allele Identifier: PA2741867147
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2818959
ClinVar RCV Id: RCV003606272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1848del
CA2739270920
NM_001351834.2:c.5542_5544del