Allele Registry

Canonical Allele Identifier: PA122612

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000013484

ClinVar Variation:

12649

HGVS (amino-acid)	Matching Registered Transcripts
NP_596870.2:p.Arg740Leu	CA122607 NM_133379.5:c.2219G>T