Canonical Allele Identifier: PA178572
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165880
ClinVar RCV Id: RCV000152243 RCV000552973 RCV002354350 RCV001704098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg20841Gln
CA178570
NM_001256850.1:c.62522G>A