Canonical Allele Identifier: PA2830216105
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr9832Ala
CA16610408
NM_133432.3:c.29494A>G