Allele Registry

Canonical Allele Identifier: PA286939

Gene: ATM HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000115230

RCV000196735

RCV000212044

RCV000587205

RCV002225324

RCV002259276

RCV003492464

RCV004549564

ClinVar Variation:

127425

1692881

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Glu2181Asp	CA286937 NM_000051.4:c.6543G>T CA382554300 NM_000051.4:c.6543G>C