Canonical Allele Identifier: PA2830191988
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser3818Asn
CA311788
NM_133378.4:c.11453G>A