Canonical Allele Identifier: PA2830224282
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 498721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg23118Trp
CA1986809
NM_133432.3:c.69352C>T