Canonical Allele Identifier: PA916032012
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys669Arg
CA166922
NM_001351834.2:c.2005T>C