Canonical Allele Identifier: PA2830213227
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala4695Thr
CA178861
NM_133432.3:c.14083G>A