Canonical Allele Identifier: PA311177
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203079
ClinVar RCV Id: RCV000185101 RCV002399689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34785Gln
CA311175
NM_001267550.2:c.104353G>C