Canonical Allele Identifier: PA2830236639
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Leu17077Phe
CA140801
NM_133437.4:c.51229C>T