Allele Registry

Canonical Allele Identifier: PA185796

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000156898

RCV000172243

RCV000310296

RCV000313729

RCV000349857

RCV000364729

RCV000400261

RCV000769929

RCV001086890

RCV002345526

RCV004544461

ClinVar Variation:

180094

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Phe25341Leu	CA185794 NM_001256850.1:c.76021T>C CA349584958 NM_001256850.1:c.76023T>G CA349584959 NM_001256850.1:c.76023T>A