Allele Registry

Canonical Allele Identifier: PA141468

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040865

RCV000172610

RCV000298721

RCV000338814

RCV000341836

RCV000387355

RCV000401107

RCV000620090

RCV000768849

RCV001081784

RCV004534949

ClinVar Variation:

47596

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Arg31107Cys	CA141465 NM_001256850.1:c.93319C>T