Canonical Allele Identifier: PA236092
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg22095Trp
CA236091
NM_001267550.2:c.66283C>T