Canonical Allele Identifier: PA916032264
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482691
ClinVar RCV Id: RCV000574798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln852Pro
CA382543755
NM_001351834.2:c.2555A>C