Canonical Allele Identifier: PA346776
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180582
ClinVar RCV Id: RCV000157578 RCV000226470 RCV000584782 RCV000727747 RCV001333492 RCV001198087 RCV001798528 RCV002469030 RCV002408710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35172del
CA346775
NM_001267550.2:c.105514_105516del