Canonical Allele Identifier: PA2830226790
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26077Ala
CA311205
NM_133432.3:c.78229A>G