Canonical Allele Identifier: PA2830213902
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332868
ClinVar RCV Id: RCV000260165 RCV000273583 RCV000319258 RCV000355350 RCV000367926 RCV002488709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Phe5900Tyr
CA10611673
NM_133432.3:c.17699T>A