Canonical Allele Identifier: PA916034499
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187077
ClinVar RCV Id: RCV000166765 RCV000197716 RCV000513206 RCV000625763 RCV002265647 RCV002485035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2606Val
CA196681
NM_001351834.2:c.7816A>G