Allele Registry

Canonical Allele Identifier: PA2825036057

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001223329

ClinVar Variation:

951419

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Asp2721Tyr	CA382562474 NM_000051.4:c.8161G>T