Allele Registry

Canonical Allele Identifier: PA2826489431

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000462788

RCV001550296

ClinVar Variation:

405030

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Arg1861Cys	CA2005162 NM_001267550.2:c.5581C>T