Allele Registry

Canonical Allele Identifier: PA2830210089

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000013484

ClinVar Variation:

12649

HGVS (amino-acid)	Matching Registered Transcripts
NP_597676.3:p.Arg694Leu	CA122607 NM_133432.3:c.2081G>T