Allele Registry

Canonical Allele Identifier: PA2825031801

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001324911

ClinVar Variation:

1024697

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Lys828Met	CA382543218 NM_000051.4:c.2483A>T