Canonical Allele Identifier: PA2573202149
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1352111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1338Asn
CA382527584
NM_001351834.2:c.4013G>A