Allele Registry

Canonical Allele Identifier: PA645500636

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000228332

RCV001014336

RCV003343712

ClinVar Variation:

236682

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Arg692His	CA6264924 NM_000051.4:c.2075G>A