Canonical Allele Identifier: PA2573203829
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1512062
ClinVar RCV Id: RCV002020728
ClinVar Variation Id: 1926595
ClinVar RCV Id: RCV002630739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala220Thr
CA382528630
NM_001351834.2:c.658G>A
CA2580083217
NM_001351834.2:c.657_658delinsCA