Canonical Allele Identifier: PA2826418632
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg17114His
CA1993284
NM_001256850.1:c.51341G>A