Allele Registry

Canonical Allele Identifier: PA138964

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000039958

RCV000269064

RCV000326449

RCV000350254

RCV000384905

RCV000388473

RCV000713986

RCV001086766

RCV001170080

RCV004534867

ClinVar Variation:

46688

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Arg5979His	CA138962 NM_133378.4:c.17936G>A