Canonical Allele Identifier: PA2741866115
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2755835
ClinVar RCV Id: RCV003500126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu574Gly
CA382535282
NM_001351834.2:c.1721A>G