Canonical Allele Identifier: PA309568
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile9921Thr
CA309566
NM_001267550.2:c.29762T>C