Canonical Allele Identifier: PA916066775
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp9166Asn
CA1993694
NM_133437.4:c.27496G>A