Canonical Allele Identifier: PA2830237673
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser18712Tyr
CA310674
NM_133437.4:c.56135C>A