Canonical Allele Identifier: PA658666142
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu19765Val
CA1992691
NM_001267550.2:c.59294A>T