Canonical Allele Identifier: PA178500
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr25375Phe
CA178498
NM_001267550.2:c.76124A>T