Canonical Allele Identifier: PA181681
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178181
ClinVar RCV Id: RCV000154908 RCV000172222 RCV000542158 RCV001170552 RCV002354370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg28322His
CA181679
NM_001267550.2:c.84965G>A