Allele Registry

Canonical Allele Identifier: PA163684

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000129025

RCV000199094

RCV000219679

RCV001199867

RCV002498640

RCV003315869

ClinVar Variation:

140832

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Arg45Trp	CA163682 NM_000051.4:c.133C>T