Canonical Allele Identifier: PA916033520
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524312
ClinVar RCV Id: RCV000628005 RCV002343182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro1843Arg
CA382545845
NM_001351834.2:c.5528C>G