Canonical Allele Identifier: PA2826426480
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 167759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30711His
CA235039
NM_001256850.1:c.92132G>A