Canonical Allele Identifier: PA645411386
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404795
ClinVar RCV Id: RCV000473870 RCV000617756 RCV001712415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr27562His
CA1989029
NM_001267550.2:c.82684T>C