Allele Registry

Canonical Allele Identifier: PA1139749122

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV001810688

RCV002430075

ClinVar Variation:

995664

HGVS (amino-acid)	Matching Registered Transcripts
NP_597681.4:p.Ile7445Leu	CA60987660 NM_133437.4:c.22333A>C