Canonical Allele Identifier: PA916065034
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Cys5507Arg
CA184461
NM_133437.4:c.16519T>C