Allele Registry

Canonical Allele Identifier: PA658801664

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000628117

ClinVar Variation:

524376

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Pro1785His	CA382543281 NM_000051.4:c.5354C>A