Canonical Allele Identifier: PA311233
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33523His
CA311232
NM_001256850.1:c.100568G>A