Canonical Allele Identifier: PA310851
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202971
ClinVar RCV Id: RCV000184962 RCV000951969 RCV001293132 RCV001170307 RCV003137740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr30305His
CA310849
NM_001267550.2:c.90913T>C