Allele Registry

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Canonical Allele Identifier: PA916033629

Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 825958

ClinVar RCV Id: RCV001024514 RCV001223920

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Gly1925Arg	CA382548292 NM_001351834.2:c.5773G>A CA382548293 NM_001351834.2:c.5773G>C