Canonical Allele Identifier: PA916031382
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826075
ClinVar RCV Id: RCV001024714 RCV001832357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys198Trp
CA382528039
NM_001351834.2:c.594C>G