Canonical Allele Identifier: PA284193
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_001254479.2:p.Ser33011Thr
CA284189
NM_001267550.2:c.99031T>A