Allele Registry

Canonical Allele Identifier: PA311167

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000185098

RCV002516953

ClinVar Variation:

203076

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Arg33057Gln	CA311166 NM_001256850.1:c.99170G>A