Allele Registry

Canonical Allele Identifier: PA645410890

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000465920

RCV000842647

ClinVar Variation:

404701

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Ile23960Thr	CA1990576 NM_001267550.2:c.71879T>C