Canonical Allele Identifier: PA2830221639
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser19128Thr
CA1988809
NM_133432.3:c.57383G>C