Canonical Allele Identifier: PA2830243025
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser26059Arg
CA311196
NM_133437.4:c.78177T>G
CA349410905
NM_133437.4:c.78177T>A
CA349410910
NM_133437.4:c.78175A>C