Canonical Allele Identifier: PA916032935
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 824556
ClinVar RCV Id: RCV001021785 RCV003605713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala1355Glu
CA382528087
NM_001351834.2:c.4064C>A