Canonical Allele Identifier: PA658668211
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp32707His
CA349434738
NM_001267550.2:c.98119G>C