Allele Registry

Canonical Allele Identifier: PA141986

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000041095

RCV000229415

RCV000619226

RCV000770112

RCV001528764

RCV001839804

RCV001839805

RCV001839806

RCV001839807

ClinVar Variation:

47826

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ile3877Phe	CA141984 NM_001256850.1:c.11629A>T