Allele Registry

Canonical Allele Identifier: PA2499251010

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001352353

ClinVar Variation:

1047615

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu762Pro	CA382539684 NM_001351834.2:c.2285T>C