Canonical Allele Identifier: PA310649
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202905
ClinVar RCV Id: RCV000184873 RCV000619230 RCV000678759 RCV001086421 RCV001706158 RCV004537555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly27101Val
CA310647
NM_001267550.2:c.81302G>T