Canonical Allele Identifier: PA2830226577
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala25885Asp
CA311181
NM_133432.3:c.77654C>A