Canonical Allele Identifier: PA2829440056
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser18520Tyr
CA310674
NM_003319.4:c.55559C>A