Allele Registry

Canonical Allele Identifier: PA122611

Gene: TTN HGNC NCBI

ClinVar Allele:

27688

ClinVar RCV:

RCV000013484

ClinVar Variation:

12649

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Arg740Leu	CA122607 NM_133378.4:c.2219G>T