Canonical Allele Identifier: PA2830202118
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 522707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp29068Asn
CA1987045
NM_133378.4:c.87202G>A