Canonical Allele Identifier: PA2830227229
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1014960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26504Ala
CA349406047
NM_133432.3:c.79510A>G