Canonical Allele Identifier: PA658667936
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro31085Leu
CA1987332
NM_001267550.2:c.93254C>T