Allele Registry

Canonical Allele Identifier: PA2825031794

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001071096

ClinVar Variation:

864006

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Phe825Val	CA382543127 NM_000051.4:c.2473T>G