Canonical Allele Identifier: PA658668223
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly32742Asp
CA1986409
NM_001267550.2:c.98225G>A