Canonical Allele Identifier: PA916031443
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 574923
ClinVar RCV Id: RCV000696987
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys241Arg
CA228384704
NM_001351834.2:c.722A>G