Canonical Allele Identifier: PA916066187
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile7790Thr
CA1994456
NM_133437.4:c.23369T>C