Canonical Allele Identifier: PA2830215019
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu7950Ala
CA309974
NM_133432.3:c.23849A>C