Canonical Allele Identifier: PA237947
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16456His
CA237945
NM_001267550.2:c.49367G>A