Canonical Allele Identifier: PA2827628560
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 485178
ClinVar RCV Id: RCV000561045 RCV000627894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln65Glu
CA6264534
NM_001351834.2:c.193C>G