Allele Registry

Canonical Allele Identifier: PA141777

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040989

RCV000082477

RCV000241675

RCV000986935

RCV001079456

RCV001128833

RCV001135821

RCV001135822

RCV001135823

RCV001171215

RCV001293191

RCV004537124

ClinVar Variation:

47720

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Met34218Thr	CA141774 NM_001256850.1:c.102653T>C