Canonical Allele Identifier: PA916032928
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 824540
ClinVar RCV Id: RCV001021757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1351Ile
CA382527911
NM_001351834.2:c.4051T>A