Canonical Allele Identifier: PA310901
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202987
ClinVar RCV Id: RCV000184981 RCV000622030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg30628Lys
CA310899
NM_001267550.2:c.91883G>A