Allele Registry

Canonical Allele Identifier: PA2829436917

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000548932

ClinVar Variation:

467398

HGVS (amino-acid)	Matching Registered Transcripts
NP_003310.4:p.Leu13269Ser	CA1991389 NM_003319.4:c.39806T>C