Canonical Allele Identifier: PA2825031427
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1783327
ClinVar RCV Id: RCV002421636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu653Ile
CA382536762
NM_000051.4:c.1957C>A