Allele Registry

Canonical Allele Identifier: PA1139728352

Gene: ATM HGNC NCBI

ClinVar Allele:

837863

ClinVar RCV:

RCV001065059

RCV004030568

ClinVar Variation:

859043

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Val2424Ala	CA382559769 NM_001351834.2:c.7271T>C