Canonical Allele Identifier: PA165787
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141561
ClinVar RCV Id: RCV000130139 RCV000466948 RCV000478287 RCV001196781
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr460Met
CA165785
NM_000051.4:c.1379C>T