Canonical Allele Identifier: PA2830222770
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala20911Asp
CA1987895
NM_133432.3:c.62732C>A