Canonical Allele Identifier: PA658667685
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467598
ClinVar RCV Id: RCV000558081 RCV001570517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly29369Asp
CA1988201
NM_001267550.2:c.88106G>A