Canonical Allele Identifier: PA916032536
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 581554
ClinVar RCV Id: RCV000705408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1035Met
CA382515133
NM_001351834.2:c.3105A>G