Canonical Allele Identifier: PA2826423539
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr25921His
CA1989029
NM_001256850.1:c.77761T>C