Allele Registry

Canonical Allele Identifier: PA2826411792

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000552228

RCV000597764

ClinVar Variation:

466690

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Arg3367Trp	CA2004190 NM_001256850.1:c.10099C>T