Canonical Allele Identifier: PA2829444794
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu25318Gln
CA181560
NM_003319.4:c.75952G>C