Canonical Allele Identifier: PA2830237156
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly17936Ser
CA140856
NM_133437.4:c.53806G>A