Canonical Allele Identifier: PA211319
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2625_Ala2626delinsGluPro
CA211317
NM_000051.4:c.7875_7876delinsGC