Canonical Allele Identifier: PA139306
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His10092Tyr
CA139304
NM_001267550.2:c.30274C>T