Canonical Allele Identifier: PA2830213686
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr5561Ser
CA1995842
NM_133432.3:c.16682C>G
CA349650320
NM_133432.3:c.16681A>T