Allele Registry

Canonical Allele Identifier: PA2826420622

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000548932

ClinVar Variation:

467398

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Leu20693Ser	CA1991389 NM_001256850.1:c.62078T>C