Canonical Allele Identifier: PA2826426807
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130686
ClinVar RCV Id: RCV000118795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg31228Pro
CA269799
NM_001256850.1:c.93683G>C