Allele Registry

Canonical Allele Identifier: PA2830195622

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV001810688

RCV002430075

ClinVar Variation:

995664

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ile13750Leu	CA60987660 NM_133378.4:c.41248A>C