Canonical Allele Identifier: PA183089
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178814
ClinVar RCV Id: RCV000155586 RCV001081292 RCV000714119 RCV002354372 RCV004534997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg30765Thr
CA183087
NM_001267550.2:c.92294G>C