Canonical Allele Identifier: PA2825031938
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2568147
ClinVar RCV Id: RCV003283513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile882Val
CA6265093
NM_000051.4:c.2644A>G