Canonical Allele Identifier: PA2826425353
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263942
ClinVar RCV Id: RCV000253675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu29004His
CA10587454
NM_001256850.1:c.87011T>A