Canonical Allele Identifier: PA2580203930
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1737660
ClinVar RCV Id: RCV002323150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1362Thr
CA382528378
NM_001351834.2:c.4085G>C