Canonical Allele Identifier: PA916034524
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3030
ClinVar RCV Id: RCV000132184 RCV000202436 RCV000679143 RCV003333722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2625_Ala2626delinsGluPro
CA211317
NM_001351834.2:c.7875_7876delinsGC