Canonical Allele Identifier: PA181725
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178191
ClinVar RCV Id: RCV000154921 RCV000621332 RCV001082619 RCV000727739 RCV000769954 RCV004534972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg22555His
CA181723
NM_001256850.1:c.67664G>A