Canonical Allele Identifier: PA916034547
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 133634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2640Ile
CA157174
NM_001351834.2:c.7919C>T