Canonical Allele Identifier: PA2826420402
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg20355Cys
CA1991600
NM_001256850.1:c.61063C>T