Canonical Allele Identifier: PA916034690
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407546
ClinVar RCV Id: RCV000564545 RCV000481130 RCV000464927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2749Arg
CA6266323
NM_001351834.2:c.8246A>G