Allele Registry

Canonical Allele Identifier: PA181922

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000154992

RCV000228841

RCV000247714

RCV000713979

RCV001353378

ClinVar Variation:

178252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Cys5940Arg	CA181920 NM_001267550.2:c.17818T>C