Allele Registry

Canonical Allele Identifier: PA181839

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000154961

RCV000172363

RCV000643341

RCV000770064

RCV001130349

RCV001130350

RCV001130351

RCV001130352

RCV001135400

ClinVar Variation:

178226

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Arg10985Trp	CA181838 NM_001267550.2:c.32953C>T