Allele Registry

Canonical Allele Identifier: PA140661

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040585

RCV000539387

RCV000727443

RCV002362634

ClinVar Variation:

47315

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Thr2160Ala	CA140658 NM_001267550.2:c.6478A>G