Canonical Allele Identifier: PA2830221299
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg18588Trp
CA310671
NM_133432.3:c.55762C>T