Allele Registry

Canonical Allele Identifier: PA311168

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000185098

RCV002516953

ClinVar Variation:

203076

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Arg34698Gln	CA311166 NM_001267550.2:c.104093G>A