Canonical Allele Identifier: PA916035153
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 629611
ClinVar RCV Id: RCV000774321 RCV001210198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Arg19Thr
CA382519285
NM_001351836.2:c.56G>C