Canonical Allele Identifier: PA916034043
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2240His
CA168417
NM_001351834.2:c.6718G>C