Canonical Allele Identifier: PA2829437092
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_003310.4:p.Asp13589His
CA140484
NM_003319.4:c.40765G>C