Canonical Allele Identifier: PA141634
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47659
ClinVar RCV Id: RCV000040928 RCV000710275 RCV000768834 RCV001133967 RCV001081893 RCV001133969 RCV001133968 RCV001133970 RCV001135483 RCV002390176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg32814Cys
CA141631
NM_001256850.1:c.98440C>T