Allele Registry

Canonical Allele Identifier: PA138948

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000039953

RCV000082370

RCV000275531

RCV000278937

RCV000333001

RCV000367843

RCV000389765

RCV001079235

RCV001170083

ClinVar Variation:

46683

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ala6805Thr	CA138945 NM_001256850.1:c.20413G>A