Allele Registry

Canonical Allele Identifier: PA181759

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000154931

RCV000293736

RCV000316262

RCV000319887

RCV000374365

RCV000389492

RCV000620398

RCV000725861

RCV001081279

RCV001293206

RCV004534973

ClinVar Variation:

178200

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Pro20204Leu	CA181757 NM_001256850.1:c.60611C>T