Canonical Allele Identifier: PA2830232922
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly10788Asp
CA140115
NM_133437.4:c.32363G>A