Canonical Allele Identifier: PA916033552
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 485218
ClinVar Variation Id: 945329
ClinVar RCV Id: RCV001215948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His1865Gln
CA382546198
NM_001351834.2:c.5595T>G
CA382546202
NM_001351834.2:c.5595T>A