Canonical Allele Identifier: PA2825034450
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2711983
ClinVar RCV Id: RCV003501329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2018del
CA2697558919
NM_000051.4:c.6053_6055del