Canonical Allele Identifier: PA311882
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203272
ClinVar RCV Id: RCV000253609 RCV000469338 RCV000727793 RCV000852903 RCV003317137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala6184Thr
CA311880
NM_001267550.2:c.18550G>A