Canonical Allele Identifier: PA2826416520
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg13096His
CA1995719
NM_001256850.1:c.39287G>A