Canonical Allele Identifier: PA178446
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165736
ClinVar RCV Id: RCV000152189 RCV001559358 RCV002362798 RCV000533851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys30893Glu
CA178444
NM_001267550.2:c.92677A>G