Canonical Allele Identifier: PA2830216589
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu10717Asp
CA1992749
NM_133432.3:c.32151A>C
CA349500202
NM_133432.3:c.32151A>T