Canonical Allele Identifier: PA2826410296
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala743Thr
CA346741
NM_001256850.1:c.2227G>A