Canonical Allele Identifier: PA181772
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178204
ClinVar RCV Id: RCV000154936 RCV000477041 RCV001589013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr17031Ile
CA181771
NM_133378.4:c.51092C>T