Canonical Allele Identifier: PA2830215925
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg9533Gly
CA310095
NM_133432.3:c.28597A>G