Canonical Allele Identifier: PA2825034261
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 959668
ClinVar RCV Id: RCV001233055 RCV002357002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn1929Ile
CA382548319
NM_000051.4:c.5786A>T