Allele Registry

Canonical Allele Identifier: PA645501138

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000474745

ClinVar Variation:

407609

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Ser854Pro	CA16613107 NM_000051.4:c.2560T>C