Canonical Allele Identifier: PA2830211230
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.His1906Arg
CA238269
NM_133432.3:c.5717A>G