Canonical Allele Identifier: PA916034158
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 133631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2332Pro
CA157165
NM_001351834.2:c.6995T>C