Canonical Allele Identifier: PA166924
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141958
ClinVar RCV Id: RCV000130699 RCV000485416 RCV000549496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys669Arg
CA166922
NM_000051.4:c.2005T>C