Canonical Allele Identifier: PA179017
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu4190Lys
CA179016
NM_133432.3:c.12568G>A