Canonical Allele Identifier: PA141021
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47443
ClinVar RCV Id: RCV000040712 RCV000227162 RCV000724198 RCV001798186 RCV002354204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile28347Thr
CA141018
NM_001267550.2:c.85040T>C