Canonical Allele Identifier: PA1139735506
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 970550
ClinVar RCV Id: RCV001246137 RCV002430043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala886Ser
CA228407514
NM_001351834.2:c.2656G>T