Canonical Allele Identifier: PA2741867658
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2679687
ClinVar RCV Id: RCV003466595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2641Lys
CA382561516
NM_001351834.2:c.7921C>A