Canonical Allele Identifier: PA139298
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46827
ClinVar RCV Id: RCV000040097 RCV000172684 RCV001078743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala9980Thr
CA139294
NM_001267550.2:c.29938G>A