Canonical Allele Identifier: PA645410989
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332783
ClinVar RCV Id: RCV000276928 RCV000325387 RCV000330878 RCV000369107 RCV000382277 RCV000469841 RCV000512928 RCV001280555 RCV002338923 RCV003150163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile24868Val
CA1990169
NM_001267550.2:c.74602A>G