Canonical Allele Identifier: PA2829445580
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr26022Met
CA344687
NM_003319.4:c.78065C>T