Canonical Allele Identifier: PA916034359
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187037
ClinVar RCV Id: RCV000166722 RCV000255700 RCV000509266 RCV000541770 RCV002247573 RCV001175362 RCV001535786
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys2488Tyr
CA196568
NM_001351834.2:c.7463G>A