Allele Registry

Canonical Allele Identifier: PA916034529

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000204776

RCV000567581

RCV003477687

RCV004547478

ClinVar Variation:

220064

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Tyr2627Cys	CA348974 NM_001351834.2:c.7880A>G