Allele Registry

Canonical Allele Identifier: PA916066027

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000184574

ClinVar Variation:

202671

HGVS (amino-acid)	Matching Registered Transcripts
NP_597681.4:p.Gly7411Glu	CA309935 NM_133437.4:c.22232G>A