Allele Registry

Canonical Allele Identifier: PA183582

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000155821

RCV000415349

RCV000726977

RCV001086291

RCV001129490

RCV001129491

RCV001129492

RCV001129493

RCV001129494

RCV002362823

RCV003486700

ClinVar Variation:

179037

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Lys31268Thr	CA183580 NM_001267550.2:c.93803A>C