Canonical Allele Identifier: PA181756
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96296
ClinVar RCV Id: RCV000154930 RCV000272166 RCV000381758 RCV000329528 RCV000468946 RCV000289674 RCV000342201 RCV000619243 RCV000852823 RCV001798281 RCV001811388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly21588Arg
CA181752
NM_001267550.2:c.64762G>A
CA349436974
NM_001267550.2:c.64762G>C