Canonical Allele Identifier: PA916033765
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481045
ClinVar RCV Id: RCV000567229 RCV001228477 RCV002248782
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2031Ile
CA382550213
NM_001351834.2:c.6092C>T