Allele Registry

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Canonical Allele Identifier: PA916033494

Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453579

ClinVar RCV Id: RCV000557051

ClinVar Variation Id: 2125329

ClinVar RCV Id: RCV003040057

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Asp1815Glu	CA382544184 NM_001351834.2:c.5445C>A CA382544186 NM_001351834.2:c.5445C>G