Canonical Allele Identifier: PA2573202178
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1352283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1358Thr
CA382528215
NM_001351834.2:c.4073G>C