Canonical Allele Identifier: PA2830234659
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg13696Gln
CA310367
NM_133437.4:c.41087G>A