Allele Registry

Canonical Allele Identifier: PA141229

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000040781

RCV000294400

RCV000307351

RCV000347053

RCV000359863

RCV000403395

RCV000723853

RCV001081378

RCV002362643

RCV003149661

RCV004541191

ClinVar Variation:

47512

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Asp27966Val	CA141227 NM_133378.4:c.83897A>T