Canonical Allele Identifier: PA310529
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202866
ClinVar RCV Id: RCV000468625 RCV000727179 RCV000765592 RCV002426899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg912Cys
CA310526
NM_001267550.2:c.2734C>T