Canonical Allele Identifier: PA2825035315
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1500225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2391Thr
CA382559554
NM_000051.4:c.7171G>A