Canonical Allele Identifier: PA2830221340
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser18645Tyr
CA310674
NM_133432.3:c.55934C>A