Canonical Allele Identifier: PA645409324
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly8761Ser
CA2000037
NM_001267550.2:c.26281G>A