Canonical Allele Identifier: PA2826410961
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg1861Cys
CA2005162
NM_001256850.1:c.5581C>T