Canonical Allele Identifier: PA302608
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192146
ClinVar RCV Id: RCV000172623 RCV001082027 RCV001293122 RCV002354443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg27937His
CA302606
NM_001256850.1:c.83810G>A