Allele Registry

Canonical Allele Identifier: PA916031779

Gene: ATM HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000131552

RCV000168391

RCV000235099

RCV000515383

RCV001067758

RCV001199851

RCV001357286

RCV003462015

RCV004551263

ClinVar Variation:

142433

861269

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338763.1:p.Trp488Cys	CA294394 NM_001351834.2:c.1464G>T CA382534152 NM_001351834.2:c.1464G>C