Canonical Allele Identifier: PA310737
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202935
ClinVar RCV Id: RCV000184913 RCV000470999 RCV002354510 RCV002492844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala28833Phe
CA310735
NM_001267550.2:c.86497_86498delinsTT