Canonical Allele Identifier: PA2580204831
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1944233
ClinVar RCV Id: RCV002650838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1902Val
CA382547860
NM_001351834.2:c.5705A>T