Allele Registry

Canonical Allele Identifier: PA2829439570

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040657

RCV000259093

RCV000466151

RCV000723773

RCV000836494

RCV001132946

RCV001132947

RCV001132948

RCV001132949

RCV001132950

RCV002345314

RCV002345491

RCV003764943

ClinVar Variation:

47387

167766

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_003310.4:p.Arg17787Cys	CA140861 NM_003319.4:c.53358_53359delinsTT CA295646 NM_003319.4:c.53359C>T