Canonical Allele Identifier: PA2829441369
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg20608Gln
CA178450
NM_003319.4:c.61823G>A