Canonical Allele Identifier: PA1139734641
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 928080
ClinVar RCV Id: RCV001191734 RCV001307691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys687Arg
CA382537484
NM_001351834.2:c.2060A>G