Canonical Allele Identifier: PA2499250932
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1011982
ClinVar RCV Id: RCV001309869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2896Pro
CA382523596
NM_001351834.2:c.8687A>C