Canonical Allele Identifier: PA2830220638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly17576Ser
CA1989460
NM_133432.3:c.52726G>A