Canonical Allele Identifier: PA2826428982
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 939688
ClinVar RCV Id: RCV001209123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr33709Ile
CA349407142
NM_001256850.1:c.101126C>T