Canonical Allele Identifier: PA310213
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202764
ClinVar RCV Id: RCV000867267 RCV001081873 RCV002453681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg19267Gln
CA310212
NM_001256850.1:c.57800G>A