Canonical Allele Identifier: PA2830239722
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr21963Pro
CA1987436
NM_133437.4:c.65887A>C