Allele Registry

Canonical Allele Identifier: PA1139735425

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001176391

RCV001230705

ClinVar Variation:

918663

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Tyr861Cys	CA382543958 NM_001351834.2:c.2582A>G