Canonical Allele Identifier: PA311153
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203071
ClinVar RCV Id: RCV000185092 RCV000462205 RCV000727152 RCV001131014 RCV001131015 RCV001130308 RCV001130307 RCV001130309 RCV002390483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile34477Thr
CA311151
NM_001267550.2:c.103430T>C