Canonical Allele Identifier: PA916034610
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 827432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2691Gly
CA382562002
NM_001351834.2:c.8071C>G