Allele Registry

Canonical Allele Identifier: PA2825031873

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV003057053

ClinVar Variation:

2124223

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asn859Asp	CA382543887 NM_000051.4:c.2575A>G