Canonical Allele Identifier: PA2830210090
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg694Ser
CA2005875
NM_133432.3:c.2080C>A