Canonical Allele Identifier: PA916033730
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2003Glu
CA382549780
NM_001351834.2:c.6009T>G
CA382549782
NM_001351834.2:c.6009T>A