Allele Registry

Canonical Allele Identifier: PA141629

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040927

RCV000619030

RCV000725429

RCV001082764

RCV001135484

RCV001135485

RCV001135486

RCV001135487

RCV001135488

RCV001170292

ClinVar Variation:

47658

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Thr32790Met	CA141626 NM_001256850.1:c.98369C>T