Canonical Allele Identifier: PA916034520
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827298
ClinVar RCV Id: RCV001026891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2623His
CA382561406
NM_001351834.2:c.7868T>A