Canonical Allele Identifier: PA658817358
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518547
ClinVar RCV Id: RCV000622125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35323Ser
CA1985183
NM_001267550.2:c.105967G>A