Canonical Allele Identifier: PA916034226
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 640794
ClinVar RCV Id: RCV000793895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2392Leu
CA382559562
NM_001351834.2:c.7175G>T