Canonical Allele Identifier: PA2826420496
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys20523Ile
CA178593
NM_001256850.1:c.61568A>T