Canonical Allele Identifier: PA211185
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130683
ClinVar RCV Id: RCV000118788 RCV000154640 RCV000242302 RCV000852795 RCV001135497 RCV001135498 RCV004529989 RCV000769887 RCV001082906 RCV001135494 RCV001135495 RCV001135496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile30213Thr
CA211182
NM_001267550.2:c.90638T>C