Allele Registry

Canonical Allele Identifier: PA141139

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040748

RCV000723789

RCV001084841

RCV001132651

RCV001132652

RCV001132653

RCV001132654

RCV001132655

RCV001170314

RCV002354217

RCV004534935

ClinVar Variation:

47479

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Val26919Met	CA141137 NM_133378.4:c.80755G>A