Canonical Allele Identifier: PA916034337
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2467Ile
CA6266107
NM_001351834.2:c.7399G>A