Allele Registry

Canonical Allele Identifier: PA2825036251

Gene: ATM HGNC NCBI

ClinVar Variation Id: 1763203

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Phe2799Leu	CA382516658 NM_000051.4:c.8395T>C CA382516674 NM_000051.4:c.8397T>A CA382516680 NM_000051.4:c.8397T>G