Allele Registry

Canonical Allele Identifier: PA2830221442

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000267737

RCV000268849

RCV000322601

RCV000328564

RCV000363314

RCV000554942

RCV001170782

RCV001565800

ClinVar Variation:

332755

HGVS (amino-acid)	Matching Registered Transcripts
NP_597676.3:p.Val18821Leu	CA1988947 NM_133432.3:c.56461G>C