Canonical Allele Identifier: PA181665
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178176
ClinVar RCV Id: RCV000154902 RCV000464472 RCV001136032 RCV001136034 RCV001136033 RCV001136035 RCV001136036 RCV002354367 RCV004534968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr29447Arg
CA181662
NM_001267550.2:c.88340C>G