Allele Registry

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Canonical Allele Identifier: PA2580203058

Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1779418

ClinVar RCV Id: RCV002407527

ClinVar Variation Id: 2070312

ClinVar RCV Id: RCV002967039

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Gln584His	CA382535375 NM_001351834.2:c.1752G>C CA382535377 NM_001351834.2:c.1752G>T