Allele Registry

Canonical Allele Identifier: PA916034232

Gene: ATM HGNC NCBI

Linked Data

ClinVar RCV:

RCV000115243

RCV000198387

RCV000487700

RCV000855569

RCV001798324

RCV002291558

RCV002370754

RCV003500739

ClinVar Variation:

127438

1757560

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Thr2396Ser	CA286969 NM_001351834.2:c.7187C>G CA382559585 NM_001351834.2:c.7186A>T