Canonical Allele Identifier: PA658801686
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_000042.3:p.Pro1843Arg
CA382545845
NM_000051.4:c.5528C>G