Canonical Allele Identifier: PA181846
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala10691Thr
CA181845
NM_001267550.2:c.32071G>A