Canonical Allele Identifier: PA2830226693
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser25992Arg
CA311196
NM_133432.3:c.77976T>G
CA349410905
NM_133432.3:c.77976T>A
CA349410910
NM_133432.3:c.77974A>C