Canonical Allele Identifier: PA2830227466
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu26757Gln
CA237596
NM_133432.3:c.80269G>C