Canonical Allele Identifier: PA310749
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu29094Lys
CA310747
NM_001267550.2:c.87280G>A