Canonical Allele Identifier: PA140008
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47101
ClinVar RCV Id: RCV000040371 RCV000555854 RCV000726968 RCV000764327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile18380Thr
CA140004
NM_001267550.2:c.55139T>C