Canonical Allele Identifier: PA658659186
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466745
ClinVar RCV Id: RCV000531836 RCV000830759 RCV004537977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val35307Ala
CA1985188
NM_001267550.2:c.105920T>C