Allele Registry

Canonical Allele Identifier: PA2825033961

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV004511100

ClinVar Variation:

3221776

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Pro1785Ser	CA382543276 NM_000051.4:c.5353C>T