Canonical Allele Identifier: PA2830223829
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala22563Thr
CA1987126
NM_133432.3:c.67687G>A