Canonical Allele Identifier: PA916034213
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142089
ClinVar RCV Id: RCV000130916 RCV000698695 RCV002492507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2374Ala
CA167374
NM_001351834.2:c.7121A>C