Canonical Allele Identifier: PA658673710
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481262
ClinVar RCV Id: RCV000570398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser421del
CA658656138
NM_000051.4:c.1261_1263del