Allele Registry

Canonical Allele Identifier: PA2825031547

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001915785

ClinVar Variation:

1406359

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ile709Asn	CA382538635 NM_000051.4:c.2126T>A