Canonical Allele Identifier: PA2826416681
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala13377Glu
CA1995514
NM_001256850.1:c.40130C>A