Canonical Allele Identifier: PA181584
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg31193Trp
CA181583
NM_133378.4:c.93577C>T