Canonical Allele Identifier: PA140486
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47258
ClinVar RCV Id: RCV000040528 RCV001135838 RCV001135839 RCV001135841 RCV001134379 RCV001135840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp20086His
CA140484
NM_133378.4:c.60256G>C