Canonical Allele Identifier: PA181892
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178242
ClinVar RCV Id: RCV000154980 RCV000172692 RCV000473052 RCV000852895 RCV001170082 RCV004534978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Cys5939Tyr
CA181891
NM_133378.4:c.17816G>A