Canonical Allele Identifier: PA1139687030
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_001254479.2:p.Thr35350Ile
CA349407142
NM_001267550.2:c.106049C>T