Allele Registry

Canonical Allele Identifier: PA2825031667

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001352353

ClinVar Variation:

1047615

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Leu762Pro	CA382539684 NM_000051.4:c.2285T>C