Canonical Allele Identifier: PA1139738725
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 861137
ClinVar RCV Id: RCV001067588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1814Trp
CA382544142
NM_001351834.2:c.5441T>G