Canonical Allele Identifier: PA1139736332
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 941834
ClinVar RCV Id: RCV001211693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1096Ser
CA382517250
NM_001351834.2:c.3287T>C