Canonical Allele Identifier: PA2499250813
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1198351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn1801Thr
CA382543744
NM_001351834.2:c.5402A>C