Canonical Allele Identifier: PA2830216606
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr10752Ala
CA1992720
NM_133432.3:c.32254A>G