Canonical Allele Identifier: PA916034500
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453705
ClinVar RCV Id: RCV000546599 RCV000777212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys2607Arg
CA382561300
NM_001351834.2:c.7819T>C