Canonical Allele Identifier: PA2830233043
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro10989Leu
CA283515
NM_133437.4:c.32966C>T