Allele Registry

Canonical Allele Identifier: PA2826498697

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV001170607

ClinVar Variation:

915637

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Leu17735Pro	CA349566042 NM_001267550.2:c.53204T>C