Allele Registry

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Canonical Allele Identifier: PA645501107

Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407558

ClinVar RCV Id: RCV000465941

ClinVar Variation Id: 1023453

ClinVar RCV Id: RCV001323495

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Glu848Asp	CA16613027 NM_000051.4:c.2544G>C CA382543668 NM_000051.4:c.2544G>T