Canonical Allele Identifier: PA2826428962
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518547
ClinVar RCV Id: RCV000622125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly33682Ser
CA1985183
NM_001256850.1:c.101044G>A