Canonical Allele Identifier: PA310730
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile28668Val
CA310728
NM_001267550.2:c.86002A>G