Allele Registry

Canonical Allele Identifier: PA183652

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000155843

RCV000536839

RCV001129119

RCV001129120

RCV001129121

RCV001131806

RCV001131807

ClinVar Variation:

179059

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ser1625Cys	CA183649 NM_133378.4:c.4874C>G