Canonical Allele Identifier: PA2826410487
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg1012Gln
CA2005663
NM_001256850.1:c.3035G>A