Canonical Allele Identifier: PA645412061
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg31060His
CA1987341
NM_001267550.2:c.93179G>A