Canonical Allele Identifier: PA284191
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47611
ClinVar RCV Id: RCV000040880 RCV000226010 RCV000246674 RCV001080938 RCV001132107 RCV001129391 RCV001132108 RCV001132109 RCV001132110 RCV001170523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser30443Thr
CA284189
NM_133378.4:c.91327T>A