Canonical Allele Identifier: PA1139729767
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 870645
ClinVar RCV Id: RCV001090200 RCV001862671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2627His
CA382561430
NM_001351834.2:c.7879T>C