Canonical Allele Identifier: PA2826416490
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 285627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg13038Gln
CA1995765
NM_001256850.1:c.39113G>A