Canonical Allele Identifier: PA2826415478
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro11089Thr
CA238045
NM_001256850.1:c.33265C>A