Canonical Allele Identifier: PA916065130
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser5691Cys
CA1995817
NM_133437.4:c.17072C>G