Canonical Allele Identifier: PA2830196332
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp15471Asn
CA1993694
NM_133378.4:c.46411G>A