Canonical Allele Identifier: PA916032907
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 418931
ClinVar RCV Id: RCV000480952 RCV003298545 RCV002525783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1332Leu
CA16619171
NM_001351834.2:c.3994A>C