Allele Registry

Canonical Allele Identifier: PA2825033941

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV001186214

ClinVar Variation:

924725

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Leu1775Phe	CA382543023 NM_000051.4:c.5325A>C CA382543026 NM_000051.4:c.5325A>T