Canonical Allele Identifier: PA2830211755
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr2497Ser
CA309149
NM_133432.3:c.7490C>G
CA349679335
NM_133432.3:c.7489A>T