Canonical Allele Identifier: PA181684
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178182
ClinVar RCV Id: RCV000154909 RCV000472564 RCV000769915 RCV000617218 RCV001134828 RCV001134829 RCV001133355 RCV001134826 RCV001134827 RCV001528765 RCV004544421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg28298Gln
CA181682
NM_001267550.2:c.84893G>A