Canonical Allele Identifier: PA2499251110
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 998937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr1835Ala
CA228389655
NM_001351834.2:c.5503A>G