Allele Registry

Canonical Allele Identifier: PA141249

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000040787

RCV000172200

RCV000472772

RCV001134952

RCV001134953

RCV001134954

RCV001134955

RCV001134956

RCV002354221

RCV003486607

ClinVar Variation:

47518

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ala29040Asp	CA141246 NM_001256850.1:c.87119C>A