Allele Registry

Canonical Allele Identifier: PA309842

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000260782

RCV000266937

RCV000310252

RCV000324442

RCV000359282

RCV000471038

RCV000725050

RCV002408819

ClinVar Variation:

202641

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ile13430Thr	CA309841 NM_001256850.1:c.40289T>C