Canonical Allele Identifier: PA1139734365
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 555577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu650del
CA658821431
NM_001351834.2:c.1948_1950del