Allele Registry

Canonical Allele Identifier: PA112631

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000013484

ClinVar Variation:

12649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Arg740Leu	CA122607 NM_001256850.1:c.2219G>T