Allele Registry

Canonical Allele Identifier: PA141469

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_001254479.2:p.Arg32748Cys	CA141465 NM_001267550.2:c.98242C>T