Allele Registry

Canonical Allele Identifier: PA140699

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040598

RCV000534367

RCV000621675

RCV000724394

RCV000852812

RCV001293173

RCV003486596

ClinVar Variation:

47328

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Asn23202Asp	CA140696 NM_001256850.1:c.69604A>G