Canonical Allele Identifier: PA141029
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47446
ClinVar RCV Id: RCV000040715 RCV000769914 RCV001080928 RCV001134723 RCV001134724 RCV001134725 RCV001134726 RCV001134727 RCV002354205 RCV003883486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser28469Cys
CA141026
NM_001267550.2:c.85406C>G