Allele Registry

Canonical Allele Identifier: PA178529

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000152226

RCV000230428

RCV000620143

RCV001132545

RCV001132546

RCV001132547

RCV001132548

RCV001133458

RCV001719940

RCV004532692

ClinVar Variation:

165854

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Ile23651Ser	CA178526 NM_001267550.2:c.70952T>G