Allele Registry

Canonical Allele Identifier: PA891845208

Gene: ATM HGNC NCBI

ClinVar Variation Id: 577267

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Phe1683Leu	CA382540436 NM_000051.4:c.5047T>C CA382540448 NM_000051.4:c.5049C>A CA382540450 NM_000051.4:c.5049C>G