Canonical Allele Identifier: PA2830202422
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp29661Asn
CA1986725
NM_133378.4:c.88981G>A