Allele Registry

Canonical Allele Identifier: PA2826413332

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000556465

RCV000595473

ClinVar Variation:

466879

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Asn6505Ser	CA2001214 NM_001256850.1:c.19514A>G