Canonical Allele Identifier: PA658674238
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453448
ClinVar RCV Id: RCV000537780 RCV000580540
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu1031Val
CA382515059
NM_000051.4:c.3092A>T