Allele Registry

Canonical Allele Identifier: PA2830208027

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000267737

RCV000268849

RCV000322601

RCV000328564

RCV000363314

RCV000554942

RCV001170782

RCV001565800

ClinVar Variation:

332755

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Val25193Leu	CA1988947 NM_133378.4:c.75577G>C