Canonical Allele Identifier: PA916034768
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 246467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2800Pro
CA10584375
NM_001351834.2:c.8399A>C