Allele Registry

Canonical Allele Identifier: PA2825031877

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001176391

RCV001230705

ClinVar Variation:

918663

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Tyr861Cys	CA382543958 NM_000051.4:c.2582A>G