Canonical Allele Identifier: PA658665977
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467283
ClinVar RCV Id: RCV000549572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys18684Tyr
CA60976860
NM_001267550.2:c.56051G>A