Canonical Allele Identifier: PA916065027
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467153
ClinVar RCV Id: RCV001131046 RCV002261109 RCV002404466 RCV000555469 RCV001131047 RCV001131048 RCV001131049 RCV001131050 RCV004527644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile5501Val
CA1995936
NM_133437.4:c.16501A>G