Canonical Allele Identifier: PA2830210100
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala698Thr
CA308962
NM_133432.3:c.2092G>A