Canonical Allele Identifier: PA2830216591
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly10721Asp
CA140115
NM_133432.3:c.32162G>A