Canonical Allele Identifier: PA2830227155
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1761050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26430Ala
CA60953427
NM_133432.3:c.79288A>G