Canonical Allele Identifier: PA179225
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg3163His
CA179222
NM_001267550.2:c.9488G>A