Allele Registry

Canonical Allele Identifier: PA284139

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040835

RCV000244854

RCV000263001

RCV000264125

RCV000298168

RCV000353168

RCV000377226

RCV001517431

ClinVar Variation:

47566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Ile32053Thr	CA284135 NM_001267550.2:c.96158T>C