Canonical Allele Identifier: PA658659284
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466773
ClinVar RCV Id: RCV000542507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile35947Val
CA349398739
NM_001267550.2:c.107839A>G