Canonical Allele Identifier: PA181599
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178164
ClinVar RCV Id: RCV000154883 RCV000172609 RCV000269738 RCV000296814 RCV000349128 RCV000242078 RCV000388775 RCV000327104 RCV001080422 RCV004544419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr32756Ile
CA181596
NM_001267550.2:c.98267C>T