Canonical Allele Identifier: PA2826417091
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 451886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu14259Lys
CA1995003
NM_001256850.1:c.42775G>A