Canonical Allele Identifier: PA916032909
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231126
ClinVar RCV Id: RCV000218774 RCV000462777 RCV000586338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1333Val
CA6265384
NM_001351834.2:c.3998A>T