Canonical Allele Identifier: PA916034501
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236780
ClinVar RCV Id: RCV000231040 RCV000573136 RCV003317161
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2609Thr
CA6266197
NM_001351834.2:c.7826T>C