Canonical Allele Identifier: PA2827630388
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3232364
ClinVar RCV Id: RCV004521044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Arg76Ile
CA382521443
NM_001351836.2:c.227G>T