Canonical Allele Identifier: PA916032387
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 489529
ClinVar RCV Id: RCV000581022 RCV001853852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser934Gly
CA6265113
NM_001351834.2:c.2800A>G