Allele Registry

Canonical Allele Identifier: PA916033830

Gene: ATM HGNC NCBI

Linked Data

ClinVar RCV:

RCV000032965

RCV000166627

RCV000258124

RCV000762825

RCV001268054

RCV001356731

RCV001762078

RCV003492323

ClinVar Variation:

39749

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Ala2067Asp	CA130514 NM_001351834.2:c.6200C>A