Canonical Allele Identifier: PA916034982
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453751
ClinVar RCV Id: RCV000529480 RCV001570885 RCV000566124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2951Ile
CA382529526
NM_001351834.2:c.8851G>A