Canonical Allele Identifier: PA2826428885
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33599Gln
CA183238
NM_001256850.1:c.100796G>A