Canonical Allele Identifier: PA344690
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr35087Met
CA344687
NM_001267550.2:c.105260C>T