Allele Registry

Canonical Allele Identifier: PA658664881

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000556465

RCV000595473

ClinVar Variation:

466879

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Asn6822Ser	CA2001214 NM_001267550.2:c.20465A>G