Allele Registry

Canonical Allele Identifier: PA181767

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000154933

RCV000243930

RCV000726451

RCV001086769

RCV001133876

RCV001133877

RCV001133878

RCV001133879

RCV001133880

RCV001170815

RCV001293232

RCV001358656

RCV004544423

ClinVar Variation:

178202

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Ala21147Thr	CA181764 NM_001267550.2:c.63439G>A