Allele Registry

Canonical Allele Identifier: PA139477

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040174

RCV000082392

RCV000309400

RCV000315049

RCV000350143

RCV000369677

RCV000399534

RCV000852870

RCV001082919

RCV001798146

ClinVar Variation:

46904

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Glu11148Asp	CA139474 NM_001256850.1:c.33444A>C CA349524450 NM_001256850.1:c.33444A>T