Canonical Allele Identifier: PA2830192259
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp4530Asn
CA2001859
NM_133378.4:c.13588G>A