Canonical Allele Identifier: PA2829444880
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_003310.4:p.Ile25412Thr
CA311151
NM_003319.4:c.76235T>C