Canonical Allele Identifier: PA2830230386
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg3321Gln
CA282632
NM_133437.4:c.9962G>A