Allele Registry

Canonical Allele Identifier: PA181917

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000154990

RCV000172696

RCV000852904

RCV001081353

RCV001130672

RCV001130673

RCV001133630

RCV001133631

RCV001133632

RCV004544429

ClinVar Variation:

178250

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Lys5792Glu	CA181915 NM_001256850.1:c.17374A>G