Canonical Allele Identifier: PA916066095
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val7564Asp
CA1994638
NM_133437.4:c.22691T>A