Canonical Allele Identifier: PA181564
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130690
ClinVar RCV Id: RCV000118803 RCV000154869 RCV000769847 RCV001086370 RCV002225083 RCV002390268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34383Gln
CA181560
NM_001267550.2:c.103147G>C