Allele Registry

Canonical Allele Identifier: PA2573071131

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001804402

ClinVar Variation:

1331886

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Leu546Met	CA382534523 NM_001351834.2:c.1636C>A