Canonical Allele Identifier: PA915986625
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 500219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly9887Val
CA1993173
NM_003319.4:c.29660G>T