Allele Registry

Canonical Allele Identifier: PA309748

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000184496

RCV000229755

ClinVar Variation:

202610

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Pro13451His	CA309746 NM_001267550.2:c.40352C>A