Canonical Allele Identifier: PA2826411149
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Cys2196Tyr
CA10581902
NM_001256850.1:c.6587G>A