Canonical Allele Identifier: PA2580204907
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1749666
ClinVar RCV Id: RCV002359774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1930Glu
CA382548328
NM_001351834.2:c.5790T>A
CA382548329
NM_001351834.2:c.5790T>G