Canonical Allele Identifier: PA1139732051
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 925962
ClinVar RCV Id: RCV001188229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu186Val
CA382527740
NM_001351834.2:c.556T>G