Allele Registry

Canonical Allele Identifier: PA237881

Gene: TTN HGNC NCBI

ClinVar Allele:

189565

ClinVar RCV:

RCV000172286

ClinVar Variation:

191922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Gly21395Cys	CA237879 NM_001267550.2:c.64183G>T