Canonical Allele Identifier: PA645410086
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229453
ClinVar RCV Id: RCV000213884 RCV000472424 RCV000997459 RCV002450636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg17223Gln
CA1994148
NM_001267550.2:c.51668G>A