Canonical Allele Identifier: PA309137
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202339
ClinVar RCV Id: RCV000184181 RCV000553885 RCV000622095 RCV000725161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34526Gln
CA309135
NM_001267550.2:c.103576G>C