Canonical Allele Identifier: PA141956
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47811
ClinVar RCV Id: RCV000041080 RCV000725031 RCV001171051 RCV001081319 RCV002399394 RCV004537137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr3653Ile
CA141953
NM_133432.3:c.10958C>T