Canonical Allele Identifier: PA658667687
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467599
ClinVar RCV Id: RCV000531701 RCV000609858 RCV002358524 RCV001507588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile29371Thr
CA1988198
NM_001267550.2:c.88112T>C