Canonical Allele Identifier: PA178905
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166105
ClinVar RCV Id: RCV000152371 RCV000515098 RCV000551047 RCV001134980 RCV001134982 RCV001134979 RCV001134981 RCV001134978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro11266Ser
CA178903
NM_001267550.2:c.33796C>T