Canonical Allele Identifier: PA916031880
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 581558
ClinVar RCV Id: RCV000705414 RCV004026690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu574Ala
CA382535281
NM_001351834.2:c.1721A>C