Canonical Allele Identifier: PA2830224302
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala23156Thr
CA141378
NM_133432.3:c.69466G>A