Canonical Allele Identifier: PA2826418555
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Cys16977Arg
CA1993375
NM_001256850.1:c.50929T>C