Canonical Allele Identifier: PA645411952
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404848
ClinVar RCV Id: RCV000475196 RCV000726797 RCV001170308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg30265Trp
CA1987742
NM_001267550.2:c.90793C>T