Canonical Allele Identifier: PA310254
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg21193Cys
CA310252
NM_001267550.2:c.63577C>T