Canonical Allele Identifier: PA2580205869
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1756080
ClinVar RCV Id: RCV003500738 RCV002378067 RCV003471359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2301Glu
CA382556964
NM_001351834.2:c.6902C>A