Canonical Allele Identifier: PA916033512
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 418035
ClinVar RCV Id: RCV000480391 RCV000566460 RCV001201482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys1838Gly
CA16619200
NM_001351834.2:c.5512T>G