Canonical Allele Identifier: PA916034128
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 661649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2308Ser
CA382557094
NM_001351834.2:c.6922G>T