Canonical Allele Identifier: PA915986647
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile9922Thr
CA1993148
NM_003319.4:c.29765T>C