Canonical Allele Identifier: PA645411039
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly25333Ser
CA1989970
NM_001267550.2:c.75997G>A