Canonical Allele Identifier: PA916066065
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg7503Cys
CA1994670
NM_133437.4:c.22507C>T