Canonical Allele Identifier: PA237733
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile29429Val
CA237731
NM_001267550.2:c.88285A>G