Canonical Allele Identifier: PA310166
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20049His
CA310164
NM_001267550.2:c.60146G>A