Canonical Allele Identifier: PA2830240978
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly23708Val
CA141439
NM_133437.4:c.71123G>T