Canonical Allele Identifier: PA2830221811
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg19424Gln
CA310716
NM_133432.3:c.58271G>A