Canonical Allele Identifier: PA181668
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178177
ClinVar RCV Id: RCV000154903 RCV000643154 RCV000622203 RCV000727801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg29293His
CA181666
NM_001267550.2:c.87878G>A