Allele Registry

Canonical Allele Identifier: PA141121

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040742

RCV000270510

RCV000327903

RCV000334082

RCV000362829

RCV000384731

RCV000475243

RCV000618175

RCV000725444

RCV001798192

ClinVar Variation:

47473

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Gly27723Ser	CA141118 NM_001256850.1:c.83167G>A