Canonical Allele Identifier: PA2830243465
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1469597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser26479Pro
CA60953469
NM_133437.4:c.79435T>C