Canonical Allele Identifier: PA916032026
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 630859
ClinVar RCV Id: RCV000776869 RCV001856137
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His683Tyr
CA382537433
NM_001351834.2:c.2047C>T