Canonical Allele Identifier: PA237598
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191806
ClinVar RCV Id: RCV000172145 RCV000220851 RCV001079372 RCV001134481 RCV001134482 RCV001134483 RCV001135937 RCV001135938 RCV002415734 RCV004539582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu35697Gln
CA237596
NM_001267550.2:c.107089G>C