Canonical Allele Identifier: PA2580205072
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1719983
ClinVar RCV Id: RCV002305071 RCV003471317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2005Val
CA382549796
NM_001351834.2:c.6013C>G