Canonical Allele Identifier: PA916033091
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met1484Thr
CA197812
NM_001351834.2:c.4451T>C