Canonical Allele Identifier: PA310190
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20495His
CA310188
NM_001267550.2:c.61484G>A