Canonical Allele Identifier: PA183642
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179056
ClinVar RCV Id: RCV000155840 RCV000179198 RCV001133776 RCV001135264 RCV001170644 RCV001133777 RCV001135263 RCV001135265 RCV001084052 RCV001293083 RCV004535002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly5848Glu
CA183639
NM_001267550.2:c.17543G>A