Canonical Allele Identifier: PA141538
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47622
ClinVar RCV Id: RCV000040891 RCV000242557 RCV000549681 RCV001131863 RCV001131862 RCV001131859 RCV001131860 RCV001131861 RCV000487595 RCV001196003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Cys31690Arg
CA141535
NM_001256850.1:c.95068T>C