Allele Registry

Canonical Allele Identifier: PA139915

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040340

RCV000172663

RCV000291245

RCV000315170

RCV000335069

RCV000350259

RCV000404069

RCV000618788

RCV000770012

RCV000852844

RCV001086451

RCV002221192

RCV004534906

ClinVar Variation:

47070

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Arg16058His	CA139912 NM_001256850.1:c.48173G>A