Canonical Allele Identifier: PA2830222442
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile20431Thr
CA1988198
NM_133432.3:c.61292T>C