Allele Registry

Canonical Allele Identifier: PA2830214659

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV002275541

ClinVar Variation:

1701398

HGVS (amino-acid)	Matching Registered Transcripts
NP_597676.3:p.Ile7318Val	CA349608043 NM_133432.3:c.21952A>G