Canonical Allele Identifier: PA2830220999
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Tyr18113Asn
CA1989244
NM_133432.3:c.54337T>A