Canonical Allele Identifier: PA2825031508
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1785498
ClinVar RCV Id: RCV002422247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys693Tyr
CA382537557
NM_000051.4:c.2078G>A