Allele Registry

Canonical Allele Identifier: PA916032305

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000166072

RCV000196727

RCV003468771

ClinVar Variation:

186472

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Pro872Leu	CA194919 NM_001351834.2:c.2615C>T