Canonical Allele Identifier: PA183122
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178832
ClinVar RCV Id: RCV000155604 RCV000474904 RCV000725227 RCV000764296 RCV000768831 RCV002399551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile34667Thr
CA183120
NM_001267550.2:c.104000T>C