Allele Registry

Canonical Allele Identifier: PA181614

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000082452

RCV000154888

RCV000263196

RCV000312560

RCV000317322

RCV000355719

RCV000369634

RCV000465970

RCV001170760

RCV002362734

RCV004529869

ClinVar Variation:

96316

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ile29189Thr	CA181612 NM_133378.4:c.87566T>C