Canonical Allele Identifier: PA916033287
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181963
ClinVar RCV Id: RCV000159730 RCV000457653 RCV000773112 RCV001798545
ClinVar Variation Id: 825305
ClinVar RCV Id: RCV001023288 RCV002550884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met1644Ile
CA298263
NM_001351834.2:c.4932G>C
CA382538133
NM_001351834.2:c.4932G>T
CA382538136
NM_001351834.2:c.4932G>A