Canonical Allele Identifier: PA141437
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30832His
CA141434
NM_001256850.1:c.92495G>A