Canonical Allele Identifier: PA2830210229
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr823Ser
CA139287
NM_133432.3:c.2467A>T
CA349496328
NM_133432.3:c.2468C>G