Canonical Allele Identifier: PA2825033151
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1739301
ClinVar RCV Id: RCV002330076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala1426Glu
CA382531333
NM_000051.4:c.4277C>A