Canonical Allele Identifier: PA1139734601
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 846132
ClinVar Variation Id: 1486360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His674Gln
CA382537351
NM_001351834.2:c.2022C>G
CA382537352
NM_001351834.2:c.2022C>A