Allele Registry

Canonical Allele Identifier: PA139882

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040327

RCV000227290

RCV000250975

RCV000279940

RCV000294783

RCV000334677

RCV000374388

RCV000389173

RCV000725456

RCV001170610

ClinVar Variation:

47057

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ser15629Ile	CA139879 NM_001256850.1:c.46886G>T