Canonical Allele Identifier: PA310369
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202813
ClinVar RCV Id: RCV000184752 RCV000220102 RCV000469752 RCV000620954 RCV004537552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg22569Gln
CA310367
NM_001267550.2:c.67706G>A