Canonical Allele Identifier: PA178704
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165965
ClinVar RCV Id: RCV000152297 RCV000226098 RCV000835240 RCV002433659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg18558His
CA178702
NM_001267550.2:c.55673G>A