Allele Registry

Canonical Allele Identifier: PA658669693

Gene: ATM HGNC NCBI

ClinVar Variation Id: 482620

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Met1909Ile	CA382547952 NM_000051.4:c.5727G>A CA382547953 NM_000051.4:c.5727G>C CA382547954 NM_000051.4:c.5727G>T